Therapy for primary and metastatic cancers

ABSTRACT

The present invention relates to compositions and methods for ablating tumor cells in a subject having at least one tumor site. More specifically, the method comprises contacting the tumor cells in at least one tumor with a lytic agent in vivo, under lytic conditions, forming a treated tumor; and applying a sufficient in vivo stimulus to the treated tumor forming a stimulated tumor. Compositions and methods are included for shrinking a local tumor or a distal metastatic tumor, or both in a subject. In a preferred embodiment, the method for shrinking a tumor in a subject comprises: contacting a stimulated tumor cells in vivo with a lytic agent. The stimulus directed toward the tumor cells is capable of increasing the level of chaperone proteins in the tumor cells. The combination of lytic agents and tumor cell stimulus leads to shrinkage of the tumors that were treated directly, wherein the stimulus is either applied simultaneously or sequentially. Moreover, distal or metastatic tumors that were not-treated directly are also decreased by introducing a lytic agents into a stimulated tumor cells in a first-tumor (“the treated tumor” or “the local tumor”). The preferred method steps that include introduction of a lytic agent and stimulation of the tumor cells is repeated in order to maximize the tumor shrinkage effects.

[0001] This application claims priority to U.S. Provisional Patent Application, Serial No. 60/443,095, entitled “Treatment for Metastatic Cancer,” filed on Jan. 28, 2003, the entire content of which is hereby incorporated by reference.

BACKGROUND

[0002] One aspect of the present invention relates to an immunotherapy for the treatment of metastatic tumors. The immunotherapeutic agents and methods of the invention relate to an administration of a physiological stress (e.g. heat) and a genetically engineered oncolytic virus directed either simultaneously or sequentially, to a treatment area, which results in subsequent tumor regression both locally and distally.

[0003] Cancer can be defined as a malignant neoplasm anywhere in the body of a person or animal. Cancer that spreads locally, or to distant parts of the body is called a metastasis. An example of the metastasis is a transfer of cells from a malignant tumor by way of the bloodstream or lymphatic fluid. There are various cancers that are characterized by the uncontrolled growth of cells that disrupt body tissue or metabolism (e.g. liver cancer, breast cancer, leukemia, etc.), wherein the proliferation destroys the adjacent tissues and finally causes death of the body by a physical block of the vessels and organs (Hanahan and Weinberg (2000). The hallmark of cancer. Cell 100.57-70). Thus, the two major characteristics of cancer cells are their immortality and their ability to form a metastasis.

[0004] I. Available treatments for cancer. Although cancer has been known for thousands of years, only recently has modem technical expertise allowed for possible treatments of cancer. Furthermore, the mechanism of action for these diverse diseases are becoming understood to the point where direct molecular intervention is possible. At present, the clinically available treatments for cancer are surgery, radiotherapy, hyperthermic therapy, chemotherapy, gene therapy, immunotherapy, and others.

[0005] Surgery. Currently, the most effective treatment of cancer still is surgery in combination with radiotherapy, chemotherapy, immunotherapy, hyperthermic therapy, etc. When cancer is diagnosed early, the 5-year survival rate after surgical treatment can be as high as 80% for various types of cancer patients. Unfortunately, in most cases the disease has already developed into late stages (stages III or IV) when patients were diagnosed. Late stage cancer cells typically have already migrated through blood or lymph vessels to distant locations throughout the body, and surgical treatment is neither practical nor effective in controlling the disease. Another drawback of a surgical treatment is that surgery cannot be applied to widespread measle-like-metastatic cancer. A further drawback to surgical treatment is the physical complications and increased risk of cancer metastasis in the patient following surgery.

[0006] Radiotherapy: Radiation therapy is a treatment used to shrink or destroy solitary cancers that cannot be safely or completely removed by surgery. It is also used to treat cancers that are not affected by chemotherapy. Radiotherapy utilizes radiation at levels thousands of times higher than the amount used to produce a chest x-ray. This intense radiation destroys the ability of cells to divide and to grow. Both normal and cancer cells are affected, but the radiation treatment is designed to maximize tumor killing effect and minimize normal tissue killing effect. Maximizing the tumor killing effect is one reason radiation therapy is given in a series of treatments rather than one treatment. In addition to cancer cells, some normal cells will also be killed by the radiation. Some side effects may be apparent because of these normal cells being killed. Usually these side effects are temporary and outweighed by the benefits of killing cancer cells. However, it is noteworthy that radiotherapy only kills cancer cells in the region that has been radiated, but does not affect cancer cells distant from the radiated region. Moreover, some specific biological features of cancer cells (e.g., resistance to radiation, size of a tumor, the proportion of anoxia cells in the cancer), may make particular cancers less susceptible to radiotherapy.

[0007] Hyperthermic therapy: Hyperthermia therapy or heat therapy, raises the temperature of whole body or a local region by various means known in the art. The hyperthermic techniques to elevate the temperature of a local region are primarily radiations in different energy range (e.g., ultrasound, microwave, radiofrequency, etc.). Although the mechanism of hyperthermia therapy for the treatment of cancer is not fully understood, hyperthermia alone or in combination with other treatments such as radiotherapy and chemotherapy have been demonstrated to have an anti-cancer effect (Falk and Issels (2001) Hyperthermia in oncology. Int. J Hyperthermia 17:1-18). Although not wanting to be bound by theory, hyperthermia changes the microenvironment of cancer cells, and leads to denaturalization and necrosis/apoptosis. Currently, there are still difficulties to optimize the conditions of hyperthermia. For example, hyperthermic treatment is difficult for deep-seated malignant tumors, and the measurement of the actual temperature distribution in the tumor and in the immediately adjacent tissues can be inconsistent. Moreover, prior art does not demonstrate that hyperthermia is effective to treat cancer distant from the site where heat is applied.

[0008] Chemotherapy: Chemotherapy is the use of an anti-cancer (cytotoxic) drug to destroy cancer cells. Currently, there are over 50 different chemotherapy drugs available. Although some chemotherapy drugs are given alone, often several drugs may be combined (i.e. combination chemotherapy). The type of specific treatment depends on many things, including the type of cancer, and how far it has spread from the origin. Chemotherapy kills fast-dividing cancer cells as well as fast-dividing normal cells such as blood cells, skin cells and gastrointestinal cells. Therefore, the application of chemical drugs to treat cancer is accompanied by severe side effects. It is also found that chemotherapy is not very effective to treat metastatic cancer. The apoptosis-resistant cancer cells are not susceptible to chemical drugs even at high doses since the mechanism for most chemical drugs is to induce the apoptosis of cancer cells.

[0009] Gene therapy: Gene therapy has developed rapidly as a new type of treatment for cancer. There are many types of vectors to deliver therapeutic genes specifically targeting cancer cells. These vectors include adenovirus vectors, adeno-associated viruses, and liposomes (Anderson (1998) Human gene therapy. Nature 392:25-30). However, various kinds of side effects and low delivering efficiency of these vectors have not yet been conquered. Hence, the clinical application of gene therapy is limited. The concept of using an oncolytic virus to treat cancer was unveiled a decade ago (Barker and Berk (1987) Adenovirus proteins from EIB reading frames are required for transformation of rodent cells by viral infection and DNA transfection. Virology 156:107-21). The clinical application of oncolytic virus has made great progress ever since, and approximately a dozen of different oncolytic viruses have entered clinical trials (Kim et al. (2001). Replication-selective virus therapy for cancer: Biological principle, risk management and future directions. Nature 7:781-787). Among these oncolytic viruses, adenovirus dl1520 has been best studied. In contrast to wild-type adenovirus, dl1520 is a variant adenovirus where a fragment of 827 bp in E1b region is deleted so that dl1520 does not express E1b-55kDa protein. The variant adenovirus dl1520 does not replicate in normal cells, but selectively replicate in cancer cells where the tumor-suppressor gene p53 is dysfunctional and eventually lyse cancer cells. The clinical trials have demonstrated that (1) oncolytic virus is safe to patients and environment; (2) the efficacy of variant adenovirus dl1520 to suppress cancer growth is not as good as expected; (3) the combined treatment of oncolytic virus dl1520 with chemical anti-cancer drugs is effective to treat cancer to some extent (Ries and Kim (2002) ONYX-015: mechanisms of action and clinical potential of a replication-selective adenovirus. British Journal of cancer 86:5-1 1). Methods and compositions for treating neoplastic conditions by viral based therapy were disclosed in U.S. Pat. No. 5,677,178 (“the McCormick '178 Patent”), titled “Cytopathic Viruses for Therapy and Prophylaxis of Neplasia,” which issued on Oct. 14, 1997 having McCormick et al., listed as inventors. In the McCormick '178 Patent, Methods and compositions for treating neoplastic conditions by viral-based therapy are provided. A mutant virus lacking viral proteins which bind and/or inactivate p53 or RB are administered to a patient having a neoplasm which comprises cells lacking p53 and/or RB function. The mutant virus is able to substantially produce a replication phenotype in neoplastic cells but is substantially unable to produce a replication phenotype in non-replicating, non-neoplastic cells having essentially normal p53 and/or RB function. The preferential generation of replication phenotype in neoplastic cells results in a preferential killing of the neoplastic cells, either directly or by expression of a cytotoxic gene in cells expressing a viral replication phenotype. However, there have been no prior art reports to demonstrate that a genetically engineered oncolytic viruses are effective to treat tumors distant from the site where viruses are administrated.

[0010] Immunotherapy: Approximately 90% of cancer patients die from metastasis, and there is virtually no effective treatments for cancer metastasis. Immunotherapy classically is a process by which an allergy patient is exposed to gradually increasing amounts of an allergen for the purpose of decreasing sensitivity to the allergen. The concept of immunotherapy for cancer treatment is based upon similar research that revealed that the immune system plays a central role in protecting the body against cancer and in combating cancer that has already developed. Although this latter role is not well understood, there is amble evidence that supports the role of the immune system to slow down the growth and spread of tumors. Although chemotherapy kills fast-dividing cancer cells as well as fast-dividing normal cells, it is able to inhibit cancer metastasis to some extent. However, the severe toxicity of chemotherapy is intolerable to most patients. It has been long thought that the patient's own immune defense system is the best way to fight cancer metastasis. At the present, the most commonly used immunotherapies can be divided into three categories: (1) immunity manipulation through administration of cytokines such as interleukins, interferons, etc; (2) immunotherapy with monoclonal antibodies specifically against one or several cancer related antigens (“CRA's”); and (3) vaccination with CRA's (Ying et al. (2001) Innovative cancer vaccine strategies based on the identification of tumor-associated antigen. BioDrugs 15:819-31).

[0011] Immunity manipulation. Interferons belong to a group of proteins known as cytokines. They are produced naturally by white blood cells in the body (or in the laboratory) in response to infection, inflammation, or stimulation. Interferon-alpha was one of the first cytokines to show an anti-tumor effect, and it is able to slow tumor growth directly, as well as help to activate the immune system. Interferon-alpha has been approved by the FDA and is now commonly used for the treatment of a number of cancers, including multiple myeloma, chronic myelogenous leukemia, hairy cell leukemia, and malignant melanoma. Interferon-beta and interferon-gamma are other types of interferons that have been investigated. Other cytokines with anti-tumor activity include the interleukins (e.g., IL-2) and tumor necrosis factor. IL-2 is frequently used to treat kidney cancer and melanoma. Since cytokines regulate cascades of specific immune responses rather than directly manipulate the immune system to specifically fight cancer, undesirable side effects are commonly observed when cytokines are used to treat cancer. Some of the problems with these cytokines, including many of the interferons and interleukins, are their side effects, which include malaise and flu-like syndromes. When given at a high dose, the side effects can be greatly magnified.

[0012] Monoclonal antibodies. Another important biological therapy involves antibodies against cancer cells or cancer-associated targets. Monoclonal antibodies are artificial antibodies against a particular target (the “antigen”) and are produced in the laboratory. The original method involved hybridoma cells (a fusion of two different types of cells) that acted as factories of antibody production. A major advance in this field was the ability to convert these antibodies, which originally were made from mouse hybridoma cells, to “humanized” antibodies that more closely resemble our natural antibodies. Even newer techniques can be used to generate human antibodies from genetically engineered mice or bacteria containing human antibody genes. Monoclonal antibodies have been widely used in scientific studies of cancer, as well as in cancer diagnosis. As therapy for cancer, monoclonal antibodies can be injected into patients to seek out the cancer cells, potentially leading to disruption of cancer cell activities or to enhancement of the immune response against the cancer. This strategy has been of great interest since the original invention of monoclonal antibodies in the 1970's. After many years of clinical testing, researchers have shown that improved monoclonal antibodies can be used effectively to help treat certain cancers. An antibody called rituximab (“Rituxan”) can be useful in the treatment of non-Hodgkin's lymphoma, while trastuzumab (“Herceptin”) is useful against certain breast cancers. Other new monoclonal antibodies are undergoing active testing. However, one of the draw backs of using monoclonal antibodies for specific types of cancer related antigens (“CRA's”) is that the types of CRA's and the amount of each type of CRA's can vary from one patient to another. Even for the same patient, the types of CRA's and the amount of each type of CRA's in the different developmental stages may be distinct. Accordingly, there are at least two drawbacks to treat cancer with monoclonal antibodies. Firstly, the efficacy is compromised if only a few of the CRA's are targeted with monoclonal antibodies. This is a particular drawback since most cancers are believed to be a multi-gene related. Secondly, different patients have different CRA's, and one or a group of specific monoclonal antibodies only will be effective for a limited number of cancer patients.

[0013] Cancer Vaccine. Although immunotherapies such as interferon and monoclonal antibodies have become part of standard cancer treatment, many other types of immunotherapy, such as cancer vaccines, remain experimental. In general, vaccines have revolutionized public health by preventing the development of many important infectious diseases, including polio, small pox, and diphtheria. However, it has been much more difficult to develop effective vaccines to prevent cancer, or to treat patients who have cancer. Despite many decades of experimental work, the attempts to develop cancer vaccines have not yielded successful results. In spite of this, a notable increase in interest has been generated by recent advances in the areas of immunology and cancer biology, which have led to more sophisticated and promising vaccine strategies than those previously available. At present, there are three basic strategies to make a cancer vaccine: (1) vaccination with one or a group of cancer related antigens (“CRA”); (2) to vaccinate a patient with dendritic cells (“DC's”) pulsed with cancer tissue lysate of the same patient; (3) to vaccinate a patient with complexes of heat shock proteins (“HSP's”) and CRA's isolated from the same patient.

[0014] (1) Vaccination with CRA. Cancer vaccines typically consist of a source of cancer related antigen (“CRA”), along with other components that further stimulate the immune response against the CRA. The challenge has been to find a better CRA, as well as to package the antigen in such a way as to enhance the patient's immune system to fight cancer cells that have the CRA. Increasingly, cancer vaccines have been shown to be capable of improving the immune response against particular antigens. The result of this immunologic effect is not always sufficient to reverse the progression of cancer. However, cancer vaccines have been generally well tolerated, and they may provide useful anticancer effects in some situations. For example, in malignant lymphoma, a number of laboratory studies have indicated that vaccination using lymphoma-associated proteins called “idiotype” can stimulate the immune systems of mice sufficiently to help them resist the development of lymphomas. In clinical trials, idiotype vaccines continue to be tested and have been associated with indications of clinical benefit in some lymphoma patients. In malignant melanoma, a wide variety of vaccine strategies have been introduced into clinical trials, and some have been found to stimulate the immune response against the cancer.

[0015] The disadvantages to vaccinate patients with one or a group of CRA's are the same as using monoclonal antibodies to treat cancer: (1) the efficacy is compromised if only a few of the CRA's are targeted; and (2) different patients have different CRA's, and (3) the resultant vaccines only will be effective for a limited number of cancer patients.

[0016] (2) Vaccination with dendritic cells (“DC's”) pulsed with cancer tissue lysate. The many new strategies for vaccine construction and immune stimulation may lead to the emergence of clinically useful cancer vaccines. An example of one exciting new approach being tested in melanoma and other cancers is the use of dendritic cell vaccines. Dendritic cells (“DC”) help to “turn on” the immune response. A dendritic cell is a type of antigen presenting cell (“APC”) characterized by its potent capacity to activate naive T cells (Banchereau,J. et al. (2000) Immunobiology of dendritic cells. Annu. Rev.Immunol. 18:767-81). By administration with DCs pulsed by CRA's in experimental animals, the cancers of these animals were diminished (Fong and Engleman (2000) Dendritic cells in cancer immunotherapy. Annu.Rev.Immunol. 18:245-273). Similar results have been demonstrated for human patients (Nestle et al. (1998) Vaccination of melanoma patients with peptide- or tumor lysate-pulsed dendritic cells. Nat.Med. 4:328-332). DC's also can be fused to cancer cells and the CRA's are pulsed into the DCs (Gong et al.(1997) Induction of anti-tumor activity by immunization with fusion of dendritic and carcinoma cells. Nat.Med.3:558-561). It has been exhibited that DC's pulsed with CRA's have the ability to suppress metastatic cancers (Kugler (2000) et al. Regression of human metastatic renal cell carcinoma after vaccination with tumor cell-dendritic cell. Nat.Med. 6:332-336). This vaccination technology is a four-step process: (1) isolation of DC's from a patient and proliferation of the isolated DC's ex vivo; (2) ex vivo manipulation of DC's maturational state; (3) ex vivo incubation of DC's with CRA's from the same patient; (4) infusion of the DC's pulsed by CRA's back to the same patient. Thus, vaccination with DC's pulsed by cancer tissue lysate from the same patient has great potential to be extremely effective to treat local cancer as well as metastatic cancer with a low risk of detrimental toxicities. Because each individual patient's whole set of CRA's are presented to the same patient's immune system, such vaccines have been called “individualized vaccines”. However, the disadvantages of individualized vaccines are (1) high-cost, (2) time-consuming, (3) sophisticated and tedious protocols of ex vivo preparation, that is often interrupted by contaminations, and (4) necessary to customize the vaccine for each individual patient, (i.e., impossible to develop a drug based on the concept of these individualized vaccines.) (Srivastava and Jaikaria (2001) Methods of purification of heat shock protein-peptide complexes for use as vaccines against cancers and infectious diseases. Methods Mol. Biol. 156:175-186).

[0017] (3)Vaccination with CRA complexed with Heat Shock Proteins (“HSP's”). The elevated expression of a group of heat shock proteins (“HSP's”), or stress proteins by any environmental stimulus including physical, chemical and biological stimuli is defined as a heat shock response or stress response. Srivastava et al. found that (1) heat shock proteins, HSP70 in particular, can bind episode peptides of cancer specific proteins to form complexes, and these complexes can be purified ex vivo; (2) infusion of these purified complexes results in that the episode peptides as CRA's complexed with HSP's migrate to DC's in vivo; (3) DC's present these CRA's to the immune system and induce immunity against cancer (Basu and Srivastava (2000) Heat shock proteins: the fountainhead of innate and adaptive immune responses. Cell Stress & Chaperones 5:443-451).

[0018] Haviv et.al. reported that HSP70 is capable to enhance the ability of oncolytic viruses to kill cultured cancer cells (Haviv et al.(2001) Heat shock and Heat shock protein 70i enhance the oncolytic effect of replicative Adenovirus. Cancer Research 61:8361-8365). However, their in vitro tests can not determine whether HSP70 may enhance the efficacy of oncolytic viruses to treat cancer without damaging the normal biological functions of animal or human. Furthermore, due to that they only did their experiments on cultured cancer cells (lung cancer lines A549, H460, and H157), they were not able to demonstrate that viral oncolysis of the cancer cells that contain high level of HSP70 would induce a systemic immune response against cancer, and consequently to treat local and metastatic cancers.

[0019] It is tempting to develop a single agent that may lead to the presentation of every cancer patient's complete set of CRA's to his/her own immune system, and induce immunity against cancer accordingly. Recently, Chen and Hu developed a viral agent that can present the whole set of almost every cancer patient's CRA's to his/her own immune system, and induce immune response against his/her own cancer (China Patent Application 01141696.3 & Pct/cn01/01616). Animal tests have demonstrated that this viral agent is effective to inhibit the growth of the treated tumor. This viral agent is an oncolytic adenovirus carrying an exogenous HSP70 gene. Although not wanting to be bound by theory, the oncolytic viruses can lyse cancer cells, and the HSP70 expressed by the viruses can capture CRA's. Following the lysis of the cancer cells that have been infected by oncolytic viruses, the CRA's complexed with HSP70 are presented to DCs, and subsequently elicit immune response against cancer cells. Although not wanting to be bound by theory, the heat shock response is a complex multi-step process, wherein HSP70 may only be one critical protein in the pathway responsible for proper presentation of the complexed CRA-HSP. Consequently, it may be necessary induce the entire set of heat shock proteins such as HSP60, HSP70, HSP90, HSP110 and so on in a treated tissue to get an adequate immune response to successfully treat metastatic cancers.

[0020] II. Currently available techniques to elevate the expression of endogenous HSP's: Although not wanting to be bound by theory, there are several known environmental stimuli that can induce a heat shock cascade in order to increase the endogenous expression of HSP. These stimuli include hyperthermia, alcohol, inhibitors of energy metabolism, heavy metals, oxidative stress, inflammation, etc (Zylicz et al.(2001) HSP70 interactions with the p53 tumor suppressor protein. The EMBO Journal 20:4634-4638). A correlation between a feverish infection and a concurrent remission from cancer has been observed, and recent publications attribute this correlation to the expression of HSP (Hobohm (2001) Fever and cancer in perspective. Cancer Immunol Immunother. 50: 391-396). Other non-toxic chemicals such as glutamine and amino acid analogs can also elevate the expression level of HSPs (Wischmeyer (2002) Glutamine and Heat Shock Protein expression. Nutrition 18:225-228; van Rijn et al.(2000) Heat shock responses by cells treated with azetidine-2-carboxylic acid. Int J Hyperthermia 16:305-318). In addition, mitochondrion uncoupling agents such as albendazole raise body temperature, and hence increase the expression of HSP's (Wallen et al.(1997) Oxidants differentially regulate the heat shock response. Int J Hyperthermia 13:517-24).

[0021] In summary, prior art has shown that it is possible to treat cancer conditions in a limited capacity utilizing various technologies and treatments, however, many of these treatments have some significant drawbacks. One aspect of the invention described herein relates to a well-timed hyperthermia applied to a malignant tumor wherein a genetically engineered oncolytic virus has also been administrated, the combination of heat and virus elicits an immune response directed against the cancer. Consequently, the combination of hyperthermia and viral oncolysis is effective to suppress the locally treated tumor as well as the distal not-treated metastasis. Another aspect of the current invention is related to other stimuli (e.g. physical, chemical or biological) that elevate the endogenous expression of HSP's in combination with viral oncolysis, wherein local treatment decrease local and distal tumors.

SUMMARY

[0022] Broadly, the present invention relates to compositions and methods for ablating tumor cells in a subject having at least one tumor site. More specifically, the method comprises contacting the tumor cells in at least one tumor with a lytic agent in vivo, under lytic conditions, forming a treated tumor; and applying a sufficient in vivo stimulus to the treated tumor forming a stimulated tumor.

[0023] One aspect of the current invention is a method for shrinking a tumor in a subject comprising the steps of: introducing a lytic agent into the tumor; once a maximum process of lysis has occurred, a stimulus is then applied to the tumor for a first period of time. The stimulus that is applied to the tumor can normally elevate the level of heat shock proteins (“HSP's”) in the tumor. The first period of time is generally about 15 minutes to 90 minutes. In a preferred embodiment, a method for shrinking a tumor includes the following method steps: (1) introducing a lytic agent into a tumor for a first number of rounds (e.g. about 1-10 rounds); (2) applying a stimulus to the tumor for a first period of time (e.g. about 15-90 minutes) starting from the second day after the first introduction of lytic agent, that can be repeated every day for a second number of rounds (e.g. about 1-20 rounds).

[0024] The method described herein can be applied to specific types of tumors. Although not wanting to be bound by theory, tumors that consist of a defective tumor-suppressor gene (e.g. defective p53), an activated oncogene (e.g. ras, or myc) are good candidates for this method of therapy. Exemplified by, but not limited to, the invention described herein is useful for a nasopharyngeal carcinoma, a breast cancer, a prostate cancer, an ovarian cancer, a malignant hepatoma, a carcinoma of esophagus, a lung cancer, a cancer of rectum, a carcinoma of stomach, a carcinoma of ovarium, a ascites, or a melanoma. In specific embodiments, the lytic agent comprises either an oncolytic virus (e.g. an adenovirus, a herpes simplex virus, a reovirus, a Newcastle disease virus, a poliovirus, a measles virus, or a vesicular stomatis virus), or an oncolytic bacterium (e.g. Salmonella, Bifidobacterium, Shigella, Listeria, Yersinia, or Clostridium), or an any type of oncolytic agent. The oncolytic virus/oncolytic bactierium can be either wild-type or genetically engineered form. Additionally, the lytic agent may comprises a therapeutic gene (e.g. an apoptotic gene, a gene for tumor necrosis, a gene for starving tumor cells to death, cytolytic gene, negative I-κ-β, caspase, γ globulin, hα-1 antitrypsin, or E1a of adenovirus).

[0025] The method step of stimulating the tumor includes: local hyperthermia; systemic hyperthermia; a high-frequency electromagnetic pulses; radiofrequency diathermy; ultrasound diathermy; an anoxia, a radiation, an alcohol, a glutamine, an infection, or an any kind of physical, chemical or biological stimulus. In a specific embodiment, local hyperthermia, is in the range of about 1 to about 7 degrees Celsius above a normal body temperature of the subject. Generally, the stimulus elevates heat shock proteins (e.g. Hsp30, Hsp60, Hsp70, Hsp90, Hsp94, Hsp96, or Hsp 110) in the stimulated tumor. By following the method of this invention, the shrinking of a tumor in a subject can be accomplished.

[0026] Another aspect of the current invention is a method for shrinking a “not-treated tumor” (or a metastasis) in a subject comprising the steps of: introducing a lytic agent into a tumor (a “treated tumor”). Once a process of lysis has occurred, a stimulus is then applied to the treated tumor. The stimulus that is applied to the treated tumor is capable of elevating the level of heat shock proteins (“HSP's”) in the treated tumor. In a preferred embodiment, a method for shrinking a not-treated tumor includes the following method steps: (1) introducing a lytic agent into a tumor (the treated tumor) for a first number of rounds (e.g. about 1-10 rounds); (2) applying a stimulus to the treated tumor for a first period of time (e.g. about 15-90 minutes) starting from the second day after the first introduction of lytic agent, that can be repeated every day for a second number of rounds (e.g. about 1-20 rounds). Not wanting to be bound by theory, the specific immunity elicited by the synchronization of introducing a lytic agent and applying a stimulus shrinks the not-treated tumors. The method described herein has been contemplated by the inventors to be applied to specific types of distal-tumors. Not wanting to be bound by theory, the treated or not-treated tumors that consist of a defective p53 tumor-suppressor gene (e.g. a defective p53), an activated oncogene (e.g. ras, or myc) are good candidates for this method of therapy. Exemplified by, but not limited to, the invention described herein is useful for a nasopharyngeal carcinoma, a breast cancer, a prostate cancer, an ovarian cancer, a malignant hepatoma, a carcinoma of esophagus, a lung cancer, a cancer of rectum, a carcinoma of stomach, a carcinoma of ovarium, a ascites, or a melanoma. In specific embodiments, the lytic agent comprises either an oncolytic virus (e.g. an adenovirus, a herpes simplex virus, a reovirus, a Newcastle disease virus, a poliovirus, a measles virus, or a vesicular stomatis virus), or an oncolytic bacterium (e.g. Salmonella, Bifidobacterium, Shigella, Listeria, Yersinia, or Clostridium), or an any type of oncolytic agent. The oncolytic virus/oncolytic bactierium can be either wild-type or genetically engineered form. Additionally, the lytic agent may comprises a therapeutic gene (e.g. an apoptotic gene, a gene for tumor necrosis, a gene for starving tumor cells to death, cytolytic gene, negative I-κ-β, caspase, γ globulin, hα-1 antitrypsin, or E1a of adenovirus).

[0027] The method step of stimulating the first-tumor was contemplated by the inventors to include: local hyperthermia; systemic hyperthermia; a high-frequency electromagnetic pulses; radiofrequency diathermy; ultrasound diathermy; an anoxia, a radiation, an alcohol, a glutamine, an infection, or an any type of stimulus. In a specific embodiment, local hyperthermia, is in the range of about 1 to about 7 degrees Celsius above a normal body temperature of the subject. Generally, the stimulus elevates heat shock proteins (e.g. Hsp30, Hsp60, Hsp70, Hsp90, Hsp94, Hsp96, or Hsp110) in the stimulated tumor. By following the method of this invention, the shrinking of a not-treated tumor in a subject can be accomplished.

BRIEF DESCRIPTION OF FIGURES

[0028]FIG. 1 shows the illustration of the genetically modified S98 adenoviruses;

[0029]FIG. 2 shows the replication of the genetically modified S98 adenoviruses in normal cells, wherein MOI abbreviates multiplicity of infection;

[0030]FIG. 3 shows an intratumoral injection dosage escalation curve for the 5 dose levels utilized for H101 (SEQID#1); and

[0031]FIG. 4 shows the number and types of tumor patients enrolled in study to determine a dosage escalation curve.

DETAILED DESCRIPTION

[0032] All of the terms used herein refer to the definitions commonly agreed by the scientific community. To insure that the terms used herein are not misinterpreted, the definitions of these terms are given as following:

[0033] The term “adjuvant” as used herein refers to a substance that can be used together with antigens, or itself can be used as antigen to elicit immunity.

[0034] The term “antigen” as used herein refers to a kind of substances that elicit immune responses, including antibody generation, activation of specific immunological cells, or the combination of the two. Antigens could be a biological macro-molecule, part of a biological macro-molecule, debris of organism, etc. .

[0035] The term “antigen presentation cell” as used herein refers to a kind of cell whose function is to process and present antigens to T cell and B cell. This type of cells includes dendritic cell, macrophage cell and B cell.

[0036] The term “cancer” as used herein refers to malignant tumor that metastasize and proliferate immortally. Cancer is a group of diseases classified by the tissues affected, and include, but are not limited to breast cancer, prostate cancer, ovarian cancer, malignant hepatoma, carcinoma of esophagus, lung cancer, cancer of rectum, nasopharyngeal carcinoma, carcinoma of stomach, pleural effusion, carcinoma of ovarium, ascites, and melanoma.

[0037] The term “cancer gene therapy” as used herein refers to that vectors carrying therapeutic gene(s) infect cancer cells, so as to destroy cancer cells. The therapeutic genes include genes related to cell apoptosis, cell lysis, cell suicide, etc. These therapeutic genes also include negative i-κ-βgene, caspase gene, γ-globulin gene, α-1 anti-trypsin gene, E1a gene for oncolytic adenovirus, etc..

[0038] The term “cancer related antigen” as used herein refers to antigen that represents the unique characteristics of cancer cells. Cancer related antigen is abbreviated as CRA.

[0039] The term “cancer vaccine” as used herein refers to a CRA or immunological cells that have encountered with CRA's. A CRA could be a molecule representing the unique characteristics of cancer cells or an episode of this type of molecule. In well-manipulated compositions, cancer vaccine may elicit patient's immunity against cancer.

[0040] The term “chaperones” as used herein refer to a group of unrelated proteins that mediate the correct folding, assembly, reparation, translocation across membranes and degradation of other proteins and simultaneously are not their functional components. One embodiment describes the “Hsp70” multi-gene family as one type of chaperones. The advantages to certain types of chaperones are characterized in specific embodiments of the invention, but they are not intended to be limiting.

[0041] The term “exogenous gene” or “trans-gene” as used herein refers to DNA sequences encoding a protein of interest inserted into a vector of gene therapy at a specific location. Exogenous gene could be from the vector itself, but had been rearranged on the genome of the vector. However, exogenous gene more often is a DNA fragment from the genome of another organism. The sequence of exogenous gene may be prepared by chemicalibiochemical synthesis, by purification from a natural source, by cloning, or by any other methods.

[0042] The term “heat shock protein” as used herein refers to a family of proteins expressed universally in almost all kinds of organisms from bacteria to human. They are also named as “stress proteins” and abbreviated as HSP's. The expression of HSP's are regulated by environmental stimuli and developmental influences, e.g., hyperthermia, anoxia, alcohol, glucose starvation (for glucose regulated proteins, or GRP's, that are also a sub-group of HSP's), tissue injury, infection, etc. HSP's play crucial roles in protein folding and protein metabolism. They may transport immunogens to DC cells that have receptors on cell membrane for HSP's. The heat shock proteins with an elevated expression level, either individually or in combination, after hyperthermic treatment include but are not limited to Hsp30, Hsp60, Hsp70, Hsp90, Hsp94, Hsp96, and Hsp110.

[0043] The term “Hsp70” as used herein refers to a multi-gene family of chaperones, but all members have a four common features: highly conserved sequence, molecular mass about 70 kDa, ATPase activity and an ability to bind and release of hydrophobic segments of unfolded polypeptide chains.

[0044] The term “lytic agent” as used herein refers a composition capable of rupturing a tumor cell.

[0045] The term “naturally-occurring” as used herein as applied to an object refers to the fact that an object can be found in nature. For example, a polypeptide or polynucleotide sequence that is present in an organism (including viruses) that can be isolated from a source in nature and which has not been intentionally modified by man in the laboratory is naturally-occurring. As used herein, the term “recombinant” indicates that a polynucleotide construct (e.g., and adenovirus genome) has been generated, in part, by intentional modification by man.

[0046] The term “not-treated tumor” as used herein refers to a tumor where oncolytic agents and environmental stimuli elevating the expression of HSP's are NOT applied directly, regardless if it is a primary tumor or a metastatic tumor. The not-treated tumor may be remote from the site of the application of oncolytic agent and the environmental stimuli elevating the expression of HSP's. The term “distal-tumor” can also be utilized interchangeably.

[0047] The term “oncolytic bacterium” as used herein refers to a genetically engineered bacterium that may replicate immortally in cancer cells, so as to kill these cancer cells. Salmonella typhimurium YS72, Bifidobacterium, Shigella, Listeria, Yersinia, Clostridium are examples, other examples are described in the article by Bermudes et al. (Bermudes et al. (2002) Live bacteria as anticancer agents and tumor-selective protein delivery vectors. Curr Opin Drug Discov Devel. 5(2):194-9.), the entire content is herein incorporated by reference.

[0048] The term “oncolytic techniques” as used herein refers to all kinds of effective protocols that can induce the lysis or death of tumor cells including apoptosis and necrosis. These protocols include application of oncolytic virus, oncolytic bacteria and any other agents that lead to the lysis or death of cancer cells.

[0049] The term “oncolytic virus” as used herein refers to a genetically engineered virus that may replicate immortally in cancer cells, so as to kill these cancer cells. Adenovirus dl1520 is an example of oncolytic viruses.

[0050] The term “p53 function” As used herein refers to the property of having an essentially normal level of a polypeptide encoded by the p53 gene (i.e., relative to non-neoplastic cells of the same histological type), wherein the p53 polypeptide is capable of binding an E1b p55 protein of wild-type adenovirus. For example, p53 function may be lost by production of an inactive (i.e., mutant) form of p53 or by a substantial decrease or total loss of expression of p53 polypeptide(s). Also, p53 function may be substantially absent in neoplastic cells, which comprise p53 alleles encoding wild-type p53 protein. For example, a genetic alteration outside of the p53 locus, such as a mutation that results in aberrant subcellular processing or localization of p53 (e.g., a mutation resulting in localization of p53 predominantly in the cytoplasm rather than the nucleus) can result in a loss of p53 function.

[0051] The terms “percentage of sequence identity” as used herein compares two optimally aligned sequences over a comparison window, wherein the portion of the sequence in the comparison window may comprise additions or deletions (i.e. “gaps”) as compared to a reference sequence for optimal alignment of the two sequences being compared. The percentage identity is calculated by determining the number of positions at which the identical residue occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window and multiplying the result by 100 to yield the percentage of sequence identity. Total identity is then determined as the average identity over all of the windows that cover the complete query sequence. Although not wanting to be bound by theory, computer software packages such as GAP, BESTFIT, BLASTA, FASTA and TFASTA can also be utilized to determine sequence identity.

[0052] The term “RB function” as used herein refers to the property of having an essentially normal level of a polypeptide encoded by the RB gene (i.e., relative to non-neoplastic cells of the same histological type), wherein the RB polypeptide is capable of binding an E1a protein of wild-type adenovirus. For example, RB function may be lost by production of an inactive (i.e., mutant) form of RB or by a substantial decrease or total loss of expression of RB polypeptide(s). Also, RB function may be substantially absent in neoplastic cells that comprise RB alleles encoding a wild-type RB protein. For example, a genetic alteration outside of the RB locus, such as a mutation that results in aberrant subcellular processing or localization of RB, may result in a loss of RB function.

[0053] The term “replication deficient virus” as used herein refers to a virus that preferentially inhibits cell proliferation or induces apoptosis in a predetermined cell population (e.g., cells substantially lacking p53 and/or RB function) which supports expression of a virus replication phenotype, and which is substantially unable to inhibit cell proliferation, induce apoptosis, or express a replication phenotype in cells comprising normal p53 and RB function levels characteristic of non-replicating, non-transformed cells. Typically, a replication deficient virus exhibits a substantial decrease in plaquing efficiency on cells comprising normal RB and/or p53 function.

[0054] The term “replication phenotype” as used herein refers to one or more of the following phenotypic characteristics of cells infected with a virus such as a replication deficient adenovirus: (1) substantial expression of late gene products, such as capsid proteins (e.g., adenoviral penton base polypeptide) or RNA transcripts initiated from viral late gene promoter(s), (2) replication of viral genomes or formation of replicative intermediates, (3) assembly of viral capsids or packaged virion particles, (4) appearance of cytopathic effect (CPE) in the infected cell, (5) completion of a viral lytic cycle, and (6) other phenotypic alterations which are typically contingent upon abrogation of p53 or RB function in non-neoplastic cells infected with a wild-type replication competent DNA virus encoding functional oncoprotein(s). A replication phenotype comprises at least one of the listed phenotypic characteristics, preferably more than one of the phenotypic characteristics.

[0055] The terms “S-98” and “H101” can be used interchangeably.

[0056] The term “stimulus” as used herein refers any action or agent that causes or changes an activity in an organism, organ, cell, or part thereof. In general, the stimulus described in specific embodiments are “in addition” to any change or impulse resulting from the introduction of the lytic agent to the tumor cells. One embodiment described herein utilizes an external hyperthermia as the stimulus. Another embodiment described herein utilizes systemic hyperthermia as the stimulus. In yet another embodiment, the stimulus utilized increases the level of chaperone proteins in the tumor cells. The advantages to certain types of stimulus are characterized in specific embodiments of the invention, but they are not intended to be limiting.

[0057] The term “treated tumor” as used herein refers to a designated tumor where oncolytic agents and environmental stimuli elevating the expression of HSP's are directly applied, no matter it is a primary tumor or a metastatic tumor. In some embodiments, the “first-tumor” is synonymous with the treated-tumor.

[0058] The term “T-lymphocyte” as used herein refers to a kind of cell that derived from thymus and can participate in a series of immune response.

[0059] The present invention relates generally to compositions and methods for ablating tumor cells in a subject having at least one tumor site. More specifically, the method comprises contacting the tumor cells in at least one tumor with a lytic agent in vivo, under lytic conditions, forming a treated tumor; and applying a sufficient in vivo stimulus to the treated tumor forming a stimulated tumor. Although not wanting to be bound by theory, the stimulated tumor expresses at least one chaperone protein at an elevated level compared to that of the tumor prior to applying the stimulus. The chaperone protein may comprises a heat shock protein (“HSP”) that binds a CRA from a lysed tumor cell and presents the CRA to the subject's immune system, whereby alerting the subject's immune system to the presence of a growing tumor.

[0060] The present invention relates to the synchronization between different kinds of oncolysis and different techniques to elevate expression of HSPs. To be more specific, this invention relates to: (1) oncolysis by a virus, a bacterium, or an any kind of agent at a designated cancer; (2) timely application of any kind of physical, chemical, or biological stimulus, e.g., hyperthermia, glutamine that elevates the expression of HSP's to the tumor where oncolytic agent was administrated so that enough HSP's capture enough CRA's to form HSP-CRA complexes; (3) the synchronization of elevated expression of HSP's and oncolysis results in sufficient release of HSP-CRA where released CRA's accurately represent the complete set of a patient's CRA's; (4) the sufficient amount of HSP-CRA is then autogenously exhibited to DC cells, and is eventually presented to the immune system; (5) the signal of HSP-CRA presented to the immune system is immunogenic enough to elicit immune response against cancer; (6) this immunological treatment for cancer can be used for both the treated tumor and the not-treated tumor, no matter whether it is a primary or metastatic cancer.

[0061] The oncolytic techniques. The development of novel cancer therapies that are selective for cancer cells with limited toxicity to normal tissues is a challenge for oncology researchers. Microorganisms, such as viruses with selectivity for tumor cells or tumor micro-environments, have been investigated as potential arsenals for decades. Genetically-modified, non-pathogenic bacteria have begun to emerge as potential antitumor agents, either to provide direct tumoricidal effects or to deliver tumoricidal molecules. Attenuated Salmonella, Clostridium and Bifidobacterium are capable of multiplying selectively in tumors and inhibiting their growth, representing a new approach for cancer treatment. Because of their selectivity for tumor tissues, these bacteria would also be ideal vectors for delivering therapeutic proteins to tumors. VNP20009, an attenuated strain of Salmonella typhimurium, and its derivative, TAPET-CD, which expresses an Escherichia coli cytosine deaminase (CD), are particularly promising, and are currently undergoing phase I clinical trials in cancer patients. (Bermudes et al. (2002) Live bacteria as anticancer agents and tumor-selective protein delivery vectors. Curr Opin Drug Discov Devel. 5(2):194-9.). Other examples of oncolytic bacteria can be exemplified by, but not limited to Salmonella, Bifidobacterium, Shigella, Listeria, Yersinia, and Clostridium.

[0062] Any viruses, bacteria, or other agents that may selectively replicate in cancer cells can be used for the purpose of oncolysis. The oncolytic viruses referred to in this invention could be herpes simplex virus (HSV-1), adenovirus, newcastle disease virus (“NDV”), poliovirus, measles virus, vesicular stomatitis virus (“VSV”), etc.

[0063] Although not wanting to be bound by theory, prior reports have demonstrated that mutation of p53 gene is one of the most common gene mutations for cancer patients. Mutations of p53 gene exist in more than half of cancer cases. One of the oncolytic techniques targeting cancers with mutation on this gene is the oncolytic virus modified from human Ad5 adenovirus with alteration in E1b region that encodes the protein E1b-55KD. This oncolytic adenovirus selectively replicates in cancer cells with p53 gene mutation, thus lyse cancer cells with high specificity. Two variant Ad5 viruses S98-001 (SEQID#1) and S98-002 (SEQID#2) with alteration in E1b region encoding for protein E1b-55kd are used as examples in this invention.

[0064] In addition, when selectively delivered to cancer cells by proper vectors, many therapeutic genes exemplified by, but not limited to genes for apoptosis, genes for cytolysis, genes for tumor necrosis, genes for starving tumor cells to death, negative I-κ-βgene, caspase gene, γ globulin gene , hα-1 anti-trypsin gene, E1a gene of adenovirus, etc may be used for the purpose of oncolysis.

[0065] The techniques to elevate expression of HSP's. Although not wanting to be bound by theory, it has been demonstrated that local hyperthermia and whole-body hyperthermia may elevate the expression of HSP's in human and animals (Li et al. (1995) Heat shock proteins, thermotolerance, and their relevance to clinical hyperthermia. Int. J. Hyperthermia 11 (4): 459-488). Accordingly, local hyperthermia (temperature range: 38° C. to 45° C.) and whole-body hyperthermia (body temperature below 42° C.) for 5 to 90 minutes were used in synchronization with oncolysis to treat local and metastatic cancers.

[0066] High-frequency electromagnetic radiation such as radiofrequency (0.1-100 MHz) diathermy and microwave (100-2,450 MHz) diathermy is most frequently used for local hyperthermia, due to its high efficiency, deep penetration, easily controlled dosage and simplicity to operate. Radiofrequency diathermy is suitable for deep-seated tumors, and microwave diathermy suits for superficial tumors. In addition, ultrasound diathermy can be used for both superficial and deep-seated tumors, though it is not appropriate for most tumors involving bone or behind gas-filled cavities, such as bowel or lung. It is noteworthy that, for this invention, hyperthermia is not used to kill local and distal cancer cells directly, but to induce the higher expression of HSP's. Additionally, the hyperthermic techniques chosen in this invention should have no impediments for the oncolytic efficiencies of oncolytic microorganisms such as oncolytic viruses, oncolytic bacteria and other vectors for gene therapy.

[0067] Although not wanting to be bound by theory, other alternatives to increase the expression of HSP's are exemplified by, but not limited to anoxia, radiation, alcohol, certain inhibitors of energy metabolism, glutamine, and any other agents that is able to elevate local or whole-body temperature and is safe to human. Any biological means that may up-regulate the expression of HSP's, e.g., heat shock transcriptional factors, infections, etc, also potentially can be used in synchronization with oncolysis to elicit immunity against cancer.

[0068] Synchronization of oncolysis and elevated expression of HSP's. The implementation protocol of this invention can be any synchronization of the above two techniques. One of the techniques to elevate the expression of HSP's synchronized with one or multiple oncolytic techniques will elicit immune response against cancer cells in order to treat primary and metastatic cancers.

[0069] One aspect of an optimized treatment for primary and metastatic cancers comprises the synchronization of hyperthermia and oncolysis by a variant adenovirus with E1b-55 KD alterations. Hyperthermia increases the expression of HSP's, and the variant adenovirus with E1b-55KD alterations lyses cancer cells selectively. When an oncolytic adenovirus lyses cancer cells at a high level, the amount of functional HSP's should also be at a high level. Only if these two “high levels” are synchronized, enough HSP-CRA's will exhibit a signal immunogenic enough to the immune system in order to elicit the immune response against cancer.

[0070] Although not wanting to be bound by theory, it has been demonstrated that (1) the optimum conditions to increase the expression of HSP's is in the temperature range of 38° C. to 45° C. and the time range of 15 to 90 minutes (Li and Mak (1985) Induction of heat shock protein synthesis in murine tumors during the development of thermotolerance. Cancer Res. 45(8):3816-3824); (2) the elevated expression of HSP's starts minutes after hyperthermic treatment ends, and the elevated level of HSP's can maintain for 24 to 48 hours (Li (1984) Thermal biology and physiology in clinical hyperthermia: current status and further needs. Cancer Res. (Suppl.) 44(8):48865-48935); (3) the inventors of this invention have determined that the maximum oncolytic effect of an oncolytic adenovirus occurs in 4 to 10 days after viral injection. Accordingly, the inventors have contemplated a protocol to maximally synchronize viral oncolysis and elevated expression of HSP's. The brief protocol comprises an outlined protocol: to inject an oncolytic adenovirus into a tumor, once a day for 5 days; and then to apply hyperthermia to the tumor of viral injection in the temperature range of 38° C. to 45° C. for 15 to 90 minutes. The hyperthermic treatment starts from the second day after the first viral injection and lasts for 8 to 16 days.

[0071] One aspect in this invention comprises an oncolytic adenovirus S98-001 (SEQID#1) with E1b-55 KD alterations that is injected into a tumor of a cancer patient, and radiofrequency diathermy (wave range at 4-24 μm, penetration range at 4-5 mm) was also subjected to the same tumor in the temperature range of 38° to 45° for 15 to 90 minutes to control the growth of the treated tumor and the growth of the not-treated tumors.

[0072] To deliver a oncolytic agent or an agent elevating the expression of HSP's, the various routes, e.g., intratumoral injection, parenteral administrations including intramuscular, intravenous and subcutaneous injections, oral administration and other systematic administrations including transdermal administrations, intranasal administrations and through suppositories can be used. The compositions can be tablet, pill, capsule, semisolid, powder, sustained release preparation, solution, suspension, aerosol or any other suitable forms. Immunity against cancer can be elicited by a composition or a pharmaceutical formula that includes both an agent for oncolysis and an agent increasing the expression of HSP's, e.g., a dosage form of an oncolytic virus and glutamine. A excipient used in the compositions can be any solid, liquid, semisolid, or gas in the presence of aerosol.

EXAMPLES

[0073] The following examples are included to demonstrate preferred embodiments of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples that follow are presented by the inventors to function well in the practice of the invention, and thus can be considered to constitute preferred modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.

Example 1

[0074] Generally, an adenovirus is in a class of viruses with double-stranded DNA genomes that cause respiratory, intestinal, and eye infections in humans or animals. The virus that causes the common cold is an adenovirus. The oncolytic viruses of this invention comprises genetically engineered adenovirus AdS variants. Specific engineered variants of AdS viruses are used for this invention and comprise S98-001 (SeqID#1) or S98-002 (SeqID#2). Although not wanting to be bound by theory, it is known that an infection of the human body with a wild-type AdS is autogenously curable. Additionally, the AdS adenovirus has been used routinely as a vector for gene therapy because there are no reports that the DNA fragments of Ad5 genome can integrate into the genome of human cells. Thus, the synchronization of injecting a specific oncolytic virus and hyperthermia to inhibit cancer at the injection site and cancers distant from the viral injection site of are utilized in this invention. Although oncolytic AdS variants are used as specific examples, other lytic agent comprises either an oncolytic virus (e.g. an adenovirus, a herpes simplex virus, a reovirus, a Newcastle disease virus, a poliovirus, a measles virus, or a vesicular stomatis virus), or an oncolytic bacterium (e.g. Salmonella, Bifidobacterium, Shigella, Listeria, Yersinia, or Clostridium), or an any type of oncolytic agent. The oncolytic virus/oncolytic bactierium can be either wild-type or genetically engineered form. Additionally, the lytic agent may comprises a therapeutic gene (e.g. an apoptotic gene, a gene for tumor necrosis, a gene for starving tumor cells to death, cytolytic gene, negative I-κ-β, caspase, γ globulin, hα-1 antitrypsin, or E1a of adenovirus).

[0075] Genetically engineered adenovirus variants S98-001 (SEQID#1) and S98-002 (SEQID#2). The genome of a wild-type Ad5 (SEQID#3) is composed of about 35,935 bps. Genetically engineered mutants of Ad5 and variants having at least 95% homology with S98-001 (SEQID#1) and S98-002 (SEQID#2), which can replicate selectively in cancer cells are considered as examples for this invention (FIG. 1). One distinction when comparing a wild-type Ad5 (SEQID#3) with the variant S98-001 (SEQID#1) is an extra TGA stop codon at position 2025 that is in E1b region of the variant. S98-001 (SEQID#1) also possesses two deletions: one is in E1b region between position 2,501 and position 3,328; the other is between position 27,865 and position 30,995 including the entire E3 region. A protein of 55 KD is encoded by the DNA sequence in E1b region. This protein is named as E1b-55 KD. In normal cells, E1b-55 KD binds and inactivates the protein encoded by the tumor-suppressor gene p53 so as to initiate virus replication. In S98-001 (SEQID#1), the two alterations in E1b region lead to the expression of a variant E1b-55 KD protein. This variant E1b-55 KD protein has very low binding affinity with P53 protein. Therefore, S98-001 (SEQID#1) is not able to replicate in normal cells. However, S98-001 (SEQID#1) replicates rapidly in cancer cells where P53 protein is dysfunctional. The function of E3 region is related to adenovirus' ability to escape from the surveillance of immune system. The complete deletion of E3 region in S98-001 (SEQID#1) enables the immune system easier to distinguish and eliminate this virus. Hence, S98-001 (SEQID# 1) is less likely to infect and to lyse normal cells comparing to the variant Ad5 viruses that only have alteration in the E1b-55 KD region. It has been demonstrated that the ratio of cytolysis between cancer cells and normal cells is in the range of about 100:1 to about 1,000: 1 for S98-001 (SEQID#1). Since S98-001 (SEQID#1) only lyses cancer cells, it is an oncolytic virus.

[0076] S98-002 (SEQID#2) is another genetically modified variant AdS. S98-002 (SEQID#2) has two deletions: one in the region encoding E1b-55 KD, between position 2501 and position 3328; and the other between position 27,865 and position 30,995 including the entire E3 region. The purpose to prepare a Ad5 variant S98-002 (SEQID#2) demonstrates another embodiment of an oncolytic adenovirus can be generated. The variant DNA sequences of Ad5 are unable to integrate into human genome, but the Ad5 variants S98-001 (SEQID#1) and S98-002 (SEQID#2) selectively replicate in cancer cells. Therefore, S98-001 (SEQID#1) and S98-002 (SEQID#2) are safe for use in humans and animals.

[0077] Preparation of oncolytic AdS variants. (1) Construction of S98 viruses. pXC-1 and pBHG1 1 were purchased from Microbix Biosystem. pXC-1 contains the adenovirus type 5 (AdS) sequence (bp22-5,790). PBHG1 1 contains the Ad5 sequence that has two deletions: bp188˜1339 in E1 region which encodes the packaging signal of the viral capsid protein; and the deletion of E3 region (bp27,865˜30,995). PBHG11 is not infective. However, co-transfection with pXC-1 and pBHG11 generates an infective virus based upon homologous recombination.

[0078] To amplify the Ad5 DNA fragment of bp1,338˜2,501 on pXC-1 by a method of PCR, the following two oligonucleotide primers were used: HZ1 (SeqID#4) (5′-CTATCCTGAGACGCCCGAC-3′), and HZ2 (SeqID#5) (5′-GATCGGATCCAGGTCTCCAGTAAGTGGTAGCTG C-3′; with the BglII site underlined).

[0079] The synthesized DNA sequence was then cloned into vector pGEM-T (Promega) to obtain the plasmid HZ102. HZ103 was constructed by ligating HZ102 Xbal/Bgl II digested fragment to pXC-1 Xbal/Bgl II digested fragment. In order to create a stop codon on pXC-1 at bp2025, plasmid HZ104 was generated with Quick Change Site Directed Mutagenesis (Strategene). The two primers used in this step were: HZ3 (SeqID#6) (5′-AAAGGATAAATGGAGTAAAGAAACC-3′), and HZ4 (SeqID#7) (5′-CAGATGGGTTTGTTCATTTATCC-3′).

[0080] The changed sequence of HZ104 had been confirmed by DNA sequencing. The HZ104 Xbal/Bgl II digested fragment was ligated to pXC-1 Xbal/Bgl II digested fragment to generate HZ105.

[0081] S98 viruses were generated using two overlapping plasmids by homologous recombination, then plaques were picked out and amplified in HYH cells. Since HYH expresses both E1A and E1B proteins normally, all of the S98 viruses can form plaques in HYH cells efficiently. Virus DNA was purified using QIAamp DNA Blood kit (Qiagen) and was analyzed by PCR and Southern blot.

[0082] Co-transfection of cell line 293 with pBHG11 and HZ105 generated S98-001 (SEQID#1). Co-transfection with pBHG11 and HZ103 generated S98-002 (SEQID#2), and co-transfection with pBHG11 and pXC-1 generated S98-100.

[0083] S98-100 has no alterations in E1b region so that it expresses E1b-55KD normally though its E3 region has been deleted. Consequently, S98-100 replicate as same as a wild-type adenovirus, i.e., S98-100 not only replicate in cancer cells, but also in normal cells. Thus, S98-100 should be considered as a wild-type S98. S98-100 was used as the positive control to determine the oncolytic specificity for S98 viruses

[0084] Two alterations in E1b region, an extra TGA stop codon at position 2025 and a deletion between position 2501 and position 3328, makes S98-001 (SEQID#1) missing part of the DNA sequence coding for protein 495R (protein E1b-55 KD) and for protein 495R synthesis related mRNA-13S, 14S and 14.5S. In the other hand, the deletion in E1b region between position 2501 and position 3328 makes S98-002 (SEQID#2) missing part of the DNA sequence coding for protein 495R (protein E1b-55 KD). Thus, S98-001 (SEQID#1) and S98-002 (SEQID#2) both selectively replicate in cancer cells where the tumor-suppressing gene p53 is dysfunctional.

[0085] In vitro plaque forming test. The in vitro plaque forming test was used to determine the growing ability of S98 viruses in p53 deficient cells. The cell lines used in this series of tests were: OVCAR-3 (oophoroma cell line, p53 deficient), Hep3B (hepatoma cell line, p53 deficient), U373 (glioma cell line, p53 deficient), SW620 (colon cancer cell line, p53 deficient), RKO (colon cancer cell line, wild type p53), HBL-100 (normal breast cell line, wild type p53).

[0086] S98-100 was used as the positive control to determine the oncolytic specificity for S98 viruses, as S98-100 replicate normally in cancer cells as well as in normal cells. Likewise, HYH was used as positive control for tested cell lines, as all of S98 viruses form plaques in HYH cells efficiently. To quantitatively compare the replication extents of S98 viruses, the plaques of S98-100 virus formed in HYH cell culture was arbitrarily defined as 100. The plaque number for other S98 viruses (“S98-XXX viruses”) in any other type of cell line (“Z”) was expressed as a percentage of the plaque numbers formed from a S98-XXX virus in cell line “Z” to the plaque number of S98-100 in HYH cells. This percentage is expressed as: ${\left( \frac{\left( {{Plaque}\quad {Number}\quad {of}\quad a\quad {S98}\text{-}{XXX}\quad {virus}\quad {in}\quad {cell}\quad {line}\text{-}{``Z"}} \right)}{\left( {{Plaque}\quad {Number}\quad {of}\quad a\quad {S98}\text{-}100\quad {virus}\quad {in}\quad {cell}\quad {line}\text{-}{``{HYH}"}} \right)} \right) \times 100} = {{Percentage}\quad {of}\quad {Plaque}\quad {Number}\quad {in}\quad {cell}\quad {line}\quad {``Z"}}$

[0087] Thus, by definition, a larger number of viral plaques represents faster virus replication. Table 1 shows that selective replication of a genetically engineered S98 adenoviruses in human cancer cells with p53 deficiency can be measured by plaques forming tests. For example, shown in Table 1, S98-001 (SEQID#1) and S98-002 (SEQID#2) replicate predominantly faster in cell lines with p53 deficiency than in cell lines without p53 deficiency. For example, S98-001 (SEQID# 1) and S98-002 (SEQID#2) replicate much more rapidly in OVCAR-3 (oophoroma cell line, p53 deficient), Hep3B (hepatoma cell line, p53 deficient), U373 (glioma cell line, p53 deficient), and SW620 (colon cancer cell line, p53 deficient) cell lines when compared to the RKO (colon cancer cell line, wild type p53) and HBL-100 (normal breast cell line, wild type p53) cell lines. Although not wanting to be bound by theory, the plaques formed in cells with normal p53 are very much limited for S98-001 (SEQID#1) and S98-002 (SEQID#2) comparing to S98-100. For example, the plaque numbers of S98-001 (SEQID#1) and S98-002 (SEQID#2) are only respectively {fraction (1/470)} and {fraction (1/250)} of that of S98-100 in RKO cells (colon cancer cell line, wild type p53). Similarly, the plaque numbers of S98-001 (SEQID#1) and S98-002 (SEQID#2) are only respectively {fraction (1/3000)} and {fraction (1/1000)} of that of S98-100 in HBL-100 cells (normal breast cell line, wild type p53). TABLE 1

[0088] The results of these plaque forming tests exhibit that (1) S98-001 (SEQID#1) and S98-002 (SEQID#2) replicate selectively in cancer cells with p53 deficiency; (2) in cells with functional p53, the replication rate of S98-001 (SEQID#1) and S98-002 (SEQID#2) is extremely low, in contrast to S98-100 that has the similar replication rate to the wild-type adenoviruses.

[0089] In vitro toxicity test. The purpose of this series of tests is to determine the toxicity of S98-001 (SEQID#1) and S98-002 (SEQID#2) to normal cells. Human mircovessel endothelium cell (hMVEC) was chosen for these tests. hMVEC is originated from human lung tissue, and it is a kind of primary cell that does not regenerate. Cells were infected with S98 viruses in gradually increasing multiplicity of infection (“MOI”), and the pathological status of the cell cultures were continuously tracked. It was demonstrated that wild-type adenoviruses lyse the monolayers of cultured hMVEC's completely in 10 days after viral infection at the MOI of 0.01. In contrast, no pathological change was observed as late as on the 10^(th) day after infection with S98-001 (SEQID#I) or S98-002 (SEQID#2) at the MOI's of 0.01, 0.1, 1.0, and 10. Thus, the toxicity of S98-001 (SEQID#1) and S98-002 (SEQID#2) to normal cells was far less than wild-type adenoviruses.

Example 2

[0090] In order to determine an effective dosing protocol for animals (e.g. including humans) to be treated with the composition and method of this invention, 5 dose levels were utilized for H101 (SEQID#1). The recombinant adenovirus was administered via intratumoral injection to patients having advanced solid tumors. One objective was to determine the Maximal Tolerated Dose (“MTD”) and safety of a intratumoral injection of H101 (SEQID#1). The five levels of H101 (SEQID#1) that were utilized are shown in Table 2 and a dosage escalation curve is shown in FIG. 3. Three patients for each of the 5 separate does levels were included. The MTD was determined to be the dose at which two patients experienced a DLT, wherein a DLT comprises a grade 4 toxicity for flu-like symptoms due to H101 (SEQID#1), a grade 4 toxicity for local reaction at the H101 (SEQID#1) injection site, or any other toxicity of grade 3 severity due to H101 (SEQID#1). If one of the three patients had a DLT, a total of 6 patients would be treated for that cohort. TABLE 2 Level H101 (virus particle) 1 5.0 × 10⁷  2 5.0 × 10⁹  3 5.0 × 10¹⁰ 4 5.0 × 10¹¹ 5 1.5 × 10¹²

[0091]FIG. 4 shows that 15 patients were enrolled with various types of tumors. Efficacy evaluation tumor assessment was performed only at the tumors injected with H101 (SEQID#1) because it is a product for local injection having 1 Partial Response (“PR”) at level of 1.5×10¹² (viral particles); 1 Minimal Response (“MR”) at level of 5.0×10¹¹ (viral particles) using non-conventional measurements.

[0092] The immune reaction after administration of H101 (SEQID#1) and the environmental impact contamination of excreted H101 was also determined. All samples taken after the administration of H101, including swabs of oropharynx, urine were negative. Plasma sample taken 4 days later after H101 administration were negative. Although not wanting to be bound by theory, these data suggest that H101 (SEQID#1) did not persist in the circulation or in the urine.

Example 3

[0093] Treatment of cancer patients using oncolytic virus S98-001 (SEQID#1) synchronized with hyperthermia. The patient's date of birth was Jun. 10, 1943. He was diagnosed “nasopharyngeal carcinoma” in 1990. After a period of treatment with radiotherapy, the progression of the primary tumor was controlled clinically. However, two tumors in the region of right neck and upper clavicle were progressing slowly during these years. In late 2001, these two tumors were treated by radiotherapy (Cobalt-60, DT 34 Gy/17F/24d) in combination with hyperthermia. Unfortunately, the progression of the two tumors was not suppressed by these treatments. This patient was hospitalized early in February 2002, and a physical examination for this patient was conducted before being treated by administration of oncolytic virus S98-001 (SEQID#1) synchronized with hyperthermia. This patient's general physical status was good, though his nasopharyngeal tissue was thickened tuberculously and engorged slightly. The surfaces of the two tumors were rough, thickened and hardened. The two tumors had the dimensions of 47×26×22 mm³ and 33×25×6 mm³ , and denoted No.1 tumor and No. 2 tumor respectively. The laboratory tests were carried out for this patient and the results of these tests are as follows: Blood Rt—normal; Urine Rt—normal; Dejection Rt—normal; Function of liver and kidney—normal, except GLO 24.2, ALT 45; Cell Immunology—normal, except CD3 60, CD4 39; X ray of chest—normal; Ultrasound—normal, except slight enlargement of spleen; ECG—complete block of right bundle; CT—two large tumors at right neck and upper clavicle, borderlines not clear.

[0094] The patient was diagnosed as: advanced nasopharyngeal carcinoma with metastasis on right shoulder and right neck. With the patients consent, he was treated by intratumoral administration of S98-001 (SEQID#1) synchronized with hyperthermia. In the course of treatment, the No. 1 tumor of the patient was injected intratumorally with S98-001 (SEQID#1) at 1.0×10¹² viral particles for 5 consecutive days starting from the first day of the course. In contrast, the No. 2 tumor was not administrated with S98-001 (SEQID#1). The No. 1 tumor was then heated locally at 41-44° C. for 90 min for 13 consecutive days starting from the 2^(nd) day of the course. A spectrum generator with the wave length at 4-24 um and penetrability at 4-5 mm was used for hyperthermia. While heating the No.1 tumor, the No.2 tumor was shielded to insure no hyperthermic treatment applied to this tumor. On the 22^(nd) day of the course, this patient's physical status was re-examined. It was found that, though the treatment including injection of S98-001 (SEQID#1) and local hyperthermia was only applied to No. 1 tumor, both the No. 1 tumor (the treated tumor) and the No. 2 tumor (the not-treated tumor) had regressed visibly. Further measurements revealed that the size of the No. 1 tumor regressed from 47×26×22 mm³ to 44×18×10 mm³ (a 70.5% reduction). More significantly, the No. 2 tumor (a not-treated tumor) also regressed from 33×25×6 mm³ to 23×17×5 mm³ (a 52.6% reduction).

[0095] Although not wanting to be bound by theory, the advantages of this invention are summarized as following: (1) complete exposure of patient's CRA's to HSP's induced by hyperthermia, and subsequent presentation of the complete set of CRA's to immune system mediated by HSP's and DCs upon cancer cell lysis by oncolytic viruses; (2) synchronous expression of HSP's and lysis of cancer cells by oncolytic viruses insuring enough signals of CRA's presented to immune system in order to elicit the immune response against cancer; (3) an entirely in vivo process bypassing the tedious procedures of the two technologies of individualized vaccination discussed previously; (4) a single agent (an oncolytic virus) in synchronization hyperthermia to elicit immunity against the complete set of CRA's of an individual tumor for every cancer patient; (5) this immunological therapy is effective for primary as well as metastatic cancers.

[0096] This case demonstrates that oncolysis in synchronization with hyperthernia is effective for a treated-tumor where the treatment is applied directly. In addition, the method is also effective for distal-tumors where a first tumor had been “treated,” but neither injection of S98-001 (SEQID#1) nor hyperthermia had been applied to the not-treated or distal-tumors.

Example 4

[0097] Chondrosarcoma. The female patient was born in 1982. In April of 2001, a tumor was found on her left lumbar and after surgery she was diagnosed as “soft tissue sarcoma.” In October 2001, the tumor relapsed and increased in size. In February 2002, the size of the tumor was 21 cm×35 cm as determined by physical examination. Pathology of a tumor biopsy showed that it was malignant tumor and a probable dediffenrentiation chondrosarcoma. A CT showed that the tumor dimensions were 15cm×11 cm with some eroded ribs nearby. Additionally, 2 metastatic lesions with dimension of 0.6×0.8cm on upper lobe of right lung were detected. After treatment with radiotherapy, a CT in March 2002 showed that tumor dimension was 13cm×11 cm, wherein the ribs nearby were eroded, and 2 metastatic lesions with dimension of 1.0×1.0 cm on upper lobe of right lung were detected. In March 2002, the patient was treated with chemotherapy with regimen as IFO 2 g dl-3+E-ADM 40 mg dl-3+DTIC 200 mg dl-5. The side effects were too severe for the patient to stand. With the patient's consent, she was treated by intratumoral administration of S98-001 synchronized with hyperthermia from July 2002. In the cycle of treatment, the tumor on left lumbar was injected intratumorally with S98-001 at 5.0×10¹¹ viral particles for 5 consecutive days starting from the first day of the cycle. Using a radiofrequency hyperthermia system operating at a frequency in the range from about 5 MHz to about 15 MHz, the injected lesion was then heated locally at 41-44° C. for 70 min for 7 consecutive days starting from the 6^(th) day of the cycle. A CT in December 2002 showed that the size of the tumor was 8.0 cm×6.0 cm (or a 66% deduction) wherein some ribs nearby were eroded. The 2 metastatic lesions with dimension of 1.0×1.0 cm on upper lobe of right lung were detected. A CT in July, 2003 showed that 2 metastatic lesions on upper lobe of right lung disappeared. This case demonstrates that oncolysis in synchronization with hyperthermia is effective for a treated-tumor where the treatment is applied directly to a primary tumor. Additionally, this example demonstrates that the composition and methods of this invention are also effective for distal-tumors (metastasis), wherein the distal-tumor was not directly injected with S98-001 and did not have hyperthermia applied.

Example 5

[0098] Non-small cell lung cancer. The male patient was born in 1933. He was diagnosed as “adenocarcinoma of right lung” after pathology test in December 2002. The phase was T3N1M1/IV having a KPS score of 60. A CT scan detected a tumor mass in the upper lobe of the lung having dimensions (3 cm×2 cm), and a metastatic lesion in the lower lobe of left lung having dimensions (1 cm×1 cm). With the patient's consent, he was treated by intratumoral administration of S98-001 synchronized with hyperthermia from January 2003. In a cycle of treatment, the tumor on right lung was injected intratumorally with S98-001 at 1.5×10¹² viral particles on day 1 and day 8 of the cycle. Using a radiofrequency hyperthermia system operating at a frequency in the range from about 5 MHz to about 15 MHz, the injected lesion was then heated locally at 41-44° C. for 2 consecutive days after the injection. After 2 cycles treatment, CT scan showed that the metastatic lesion in the lower lobe of left lung disappeared, the injected lesion stayed stable. CT of the visit in October, 2003 showed that the metastatic lesion in the lower lobe of left lung disappeared showing a complete response (“CR”), wherein the objective response of the injected lesion having dimensions of (3 cm×1 cm with a 50% reduction in size) was a partial response (“PR”). This case demonstrates that oncolysis in synchronization with hyperthermia is effective for a treated-tumor where the treatment is applied directly to the tumor. Additionally, the method is also effective for distal-tumors.

Example 6

[0099] Colon cancer. The male patient was born in 1983. He was diagnosed as “cancer of colon (sigmoid), small intestine and pelvic cavity invasion, Duke's D and moderate differentiated adenocarcinoma,” after radical surgery in April 2001. After surgery, from July 2001 to April 2002, he was treated with chemotherapy, wherein 5-FU, CDDP, MMC was used, together with levamisole, capecitabine, CPT-11, Taxus chinensis compound and Coix lachrymajobi oil. In October 2002, a metastatic lesion on his abdominal wall was found with the size of 3.5 cm×5.0 cm, along with the symptoms of incomplete intestinal obstruction. With the patient's consent, he was treated by intratumoral administration of S98-001 synchronized with hyperthermia from November 12^(th) to November 18^(th), 2002. In a cycle of treatment, the primary tumor was injected intratumorally with S98-001 at 1.5×10¹² viral particles. The injected lesion was then heated locally at 41-44° C. for 70 min for 2 consecutive days after the injection. From Nov. 21, 2002, low dosage chemotherapy was used with the regimen 5-FU 0.3 24h d1˜5+DDP 5 mg d1˜5+CPT-11 0.1 d1,8 for 4 cycles. There were 3 weeks included in one cycle. A CT on Oct. 28, 2002 showed an abdominal wall lesion having dimensions 3.5×5.0 cm, rectal region tumor 1.2 cm×1.0 cm (before treatment). On Dec. 30, 2002 showed the abdominal wall lesion had been reduced to 3.7 cm×2.0 cm and the rectal region tumor having dimensions 1.2×1.0 cm. A CT on Feb. 11, 2003 showed: abdominal wall lesion had been reduced to 2 cm×2.5 cm and the rectal region tumor had been reduced to 1.2 cm×1.4 cm. CT's on Jan. 20, 2003 and a fine needle biopsy of the areas on Feb. 21, 2003 showed that both the abdominal wall lesion and the rectal region tumor were only proliferation of granulation tissue and no cancer cells were found. Symptoms of the patient were relieved and he went on normal diet. This case demonstrates that oncolysis in synchronization with hyperthermia is effective for a treated-tumor where the treatment is applied directly. In addition, the method is also effective for distal-tumors.

[0100] Although not wanting to be bound by theory, the advantages of the compositions and methods of this invention are summarized as following: (1) complete exposure of patient's CRA's to HSP's induced by hyperthermia, and subsequent presentation of the complete set of CRA's to immune system mediated by HSP's and DCs upon cancer cell lysis by oncolytic viruses; (2) synchronous expression of HSP's and lysis of cancer cells by oncolytic viruses insuring enough signals of CRA's presented to immune system in order to elicit the immune response against cancer; (3) an entirely in vivo process bypassing the tedious procedures of the two technologies of individualized vaccination discussed previously; (4) a single agent (an oncolytic virus) in synchronization hyperthermia to elicit immunity against the complete set of CRA's of an individual tumor for every cancer patient; (5) this immunological therapy is effective for primary as well as metastatic cancers.

[0101] References Cited

[0102] The following U.S. Pat. No. documents and publications are incorporated by reference herein.

[0103] U.S. Patent Documents

[0104] U.S. Pat. No. 5,677,178 issued in October 1997 with McCormick, et al. listed as inventors.

[0105] U.S. Pat. No. 5,750,119 issued in May of 1998 with Srivastava, et al. listed as inventors.

[0106] U.S. Pat. No. 5,788,963 issued in August of 1998 with Murphy, et al. listed as inventors.

[0107] U.S. Pat. No. 6,017,540 issued in January of 2000 with Srivastava, et al. listed as inventors.

[0108] Other Publications

[0109] Alemany et al. (2000) Replicative adenoviruses for cancer therapy. Nature Biotechnology 18:723-727

[0110] Anderson (1998) Human gene therapy. Nature 392:25-30

[0111] Banchereau et al. (2000) Immunobiology of dendritic cells. Annu. Rev.Immunol. 18:767-81

[0112] Barker and Berk (1987) Adenovirus proteins from E1B reading frames are required for transformation of rodent cells by viral infection and DNA transfection. Virology 156:107-21

[0113] Bischoff et al. (1999) An adenovirus mutant that replicates selectively in p53-deficient human tumor cells. Science 274:373-6

[0114] Basu and Srivastava (2000) Heat shock proteins: the fountainhead of innate and adaptive immune responses. Cell Stress & Chaperones 5:443-451

[0115] Bermudes et al. (2002) Live bacteria as anticancer agents and tumor-selective protein delivery vectors. Curr Opin Drug Discov Devel. 5(2): 194-9

[0116] Falk and Issels (2001) Hyperthermia in oncology. Int. J. Hyperthermia 17:1-18

[0117] Fong and Engleman (2000) Dendritic cells in cancer immunotherapy. Annu.Rev.Immunol. 18:245-273

[0118] Gong et al.(1997) Induction of anti-tumor activity by immunization with fusion of dendritic and carcinoma cells. Nat.Med.3:558-561

[0119] Hanahan and Weinberg (2000). The hallmark of cancer. Cell 100.57-70

[0120] Haviv et al.(2001) Heat shock and Heat shock protein 70i enhance the oncolytic effect of replicative Adenovirus. Cancer Research 61:8361-8365

[0121] Hawkins et al. (2002) Oncolytic biotherapy: a novel therapeutic platform. The Lancet Oncology 3:17-26

[0122] Hobohm (2001) Fever and cancer in perspective. Cancer Immunol Immunother.50: 391-396

[0123] Kim et al. (2001). Replication-selective virus therapy for cancer: Biological principle, risk management and future directions. Nature 7:781-787

[0124] Kugler et al. (2000) Regression of human metastatic renal cell carcinoma after vaccination with tumor cell-dendritic cell. Nat.Med.6:332-336

[0125] Li (1984) Thermal biology and physiology in clinical hyperthermia: current status and further needs. Cancer Res. (Suppl.) 44(8):48865-48935

[0126] Li and Mak (1985) Induction of heat shock protein synthesis in murine tumors during the development of thermotolerance. Cancer Res. 45(8):3816-3824

[0127] Li et al. (1995) Heat shock proteins, thermotolerance, and their relevance to clinical hyperthermia. Int. J. Hyperthermia 11(4): 459-488

[0128] Lindquist and Craig (1988) The heat-shock proteins. Annu Rev Genet;22:631-77.

[0129] Nestle et al. 1998 Vaccination of melanoma patients with peptide- or tumor lysate-pulsed dendritic cells. Nat.Med.4:328-332

[0130] Ries and Kim (2002) ONYX-015: mechanisms of action and clinical potential of a replication-selective adenovirus. British Journal of cancer 86:5-11

[0131] Srivastava and Jaikaria (2001) Methods of purification of heat shock protein-peptide complexes for use as vaccines against cancers and infectious diseases. Methods Mol. Biol. 156:175-186

[0132] van Rijn et al.(2000) Heat shock responses by cells treated with azetidine-2-carboxylic acid. Int J Hyperthermia 16:305-318

[0133] Wallen et al.(1997) Oxidants differentially regulate the heat shock response. Int J Hyperthermia 13:517-24

[0134] Welch (1992) Mammalian stress response: cell physiology, structure/function of stress proteins, and implications for medicine and disease. Physiol Rev 72(4):1063-81.

[0135] Wischmeyer (2002) Glutamine and Heat Shock Protein expression. Nutrition 18:225-228

[0136] Ying et al. (2001) Innovative cancer vaccine strategies based on the identification of tumor-associated antigen. BioDrugs 15:819-31

[0137] Zylicz et al.(2001) HSP70 interactions with the p53 tumor suppressor protein. EMBO Journal 20:4634-4638

1 8 1 31976 DNA Adenovirus 1 catcatcaat aatatacctt attttggatt gaagccaata tgataatgag ggggtggagt 60 ttgtgacgtg gcgcggggcg tgggaacggg gcgggtgacg tagtagtgtg gcggaagtgt 120 gatgttgcaa gtgtggcgga acacatgtaa gcgacggatg tggcaaaagt gacgtttttg 180 gtgtgcgccg gtgtacacag gaagtgacaa ttttcgcgcg gttttaggcg gatgttgtag 240 taaatttggg cgtaaccgag taagatttgg ccattttcgc gggaaaactg aataagagga 300 agtgaaatct gaataatttt gtgttactca tagcgcgtaa tatttgtcta gggccgcggg 360 gactttgacc gtttacgtgg agactcgccc aggtgttttt ctcaggtgtt ttccgcgttc 420 cgggtcaaag ttggcgtttt attattatag tcagctgacg tgtagtgtat ttatacccgg 480 tgagttcctc aagaggccac tcttgagtgc cagcgagtag agttttctcc tccgagccgc 540 tccgacaccg ggactgaaaa tgagacatat tatctgccac ggaggtgtta ttaccgaaga 600 aatggccgcc agtcttttgg accagctgat cgaagaggta ctggctgata atcttccacc 660 tcctagccat tttgaaccac ctacccttca cgaactgtat gatttagacg tgacggcccc 720 cgaagatccc aacgaggagg cggtttcgca gatttttccc gactctgtaa tgttggcggt 780 gcaggaaggg attgacttac tcacttttcc gccggcgccc ggttctccgg agccgcctca 840 cctttcccgg cagcccgagc agccggagca gagagccttg ggtccggttt ctatgccaaa 900 ccttgtaccg gaggtgatcg atcttacctg ccacgaggct ggctttccac ccagtgacga 960 cgaggatgaa gagggtgagg agtttgtgtt agattatgtg gagcaccccg ggcacggttg 1020 caggtcttgt cattatcacc ggaggaatac gggggaccca gatattatgt gttcgctttg 1080 ctatatgagg acctgtggca tgtttgtcta cagtaagtga aaattatggg cagtgggtga 1140 tagagtggtg ggtttggtgt ggtaattttt tttttaattt ttacagtttt gtggtttaaa 1200 gaattttgta ttgtgatttt tttaaaaggt cctgtgtctg aacctgagcc tgagcccgag 1260 ccagaaccgg agcctgcaag acctacccgc cgtcctaaaa tggcgcctgc tatcctgaga 1320 cgcccgacat cacctgtgtc tagagaatgc aatagtagta cggatagctg tgactccggt 1380 ccttctaaca cacctcctga gatacacccg gtggtcccgc tgtgccccat taaaccagtt 1440 gccgtgagag ttggtgggcg tcgccaggct gtggaatgta tcgaggactt gcttaacgag 1500 cctgggcaac ctttggactt gagctgtaaa cgccccaggc cataaggtgt aaacctgtga 1560 ttgcgtgtgt ggttaacgcc tttgtttgct gaatgagttg atgtaagttt aataaagggt 1620 gagataatgt ttaacttgca tggcgtgtta aatggggcgg ggcttaaagg gtatataatg 1680 cgccgtgggc taatcttggt tacatctgac ctcatggagg cttgggagtg tttggaagat 1740 ttttctgctg tgcgtaactt gctggaacag agctctaaca gtacctcttg gttttggagg 1800 tttctgtggg gctcatccca ggcaaagtta gtctgcagaa ttaaggagga ttacaagtgg 1860 gaatttgaag agcttttgaa atcctgtggt gagctgtttg attctttgaa tctgggtcac 1920 caggcgcttt tccaagagaa ggtcatcaag actttggatt tttccacacc ggggcgcgct 1980 gcggctgctg ttgctttttt gagttttata aaggataaat ggagtgaaga aacccatctg 2040 agcggggggt acctgctgga ttttctggcc atgcatctgt ggagagcggt tgtgagacac 2100 aagaatcgcc tgctactgtt gtcttccgtc cgcccggcga taataccgac ggaggagcag 2160 cagcagcagc aggaggaagc caggcggcgg cggcaggagc agagcccatg gaacccgaga 2220 gccggcctgg accctcggga atgaatgttg tacaggtggc tgaactgtat ccagaactga 2280 gacgcatttt gacaattaca gaggatgggc aggggctaaa gggggtaaag agggagcggg 2340 gggcttgtga ggctacagag gaggctagga atctagcttt tagcttaatg accagacacc 2400 gtcctgagtg tattactttt caacagatca aggataattg cgctaatgag cttgatctgc 2460 tggcgcagaa gtattccata gagcagctga ccacttactg gagatctgga aggtgctgag 2520 gtacgatgag acccgcacca ggtgcagacc ctgcgagtgt ggcggtaaac atattaggaa 2580 ccagcctgtg atgctggatg tgaccgagga gctgaggccc gatcacttgg tgctggcctg 2640 cacccgcgct gagtttggct ctagcgatga agatacagat tgaggtactg aaatgtgtgg 2700 gcgtggctta agggtgggaa agaatatata aggtgggggt cttatgtagt tttgtatctg 2760 ttttgcagca gccgccgccg ccatgagcac caactcgttt gatggaagca ttgtgagctc 2820 atatttgaca acgcgcatgc ccccatgggc cggggtgcgt cagaatgtga tgggctccag 2880 cattgatggt cgccccgtcc tgcccgcaaa ctctactacc ttgacctacg agaccgtgtc 2940 tggaacgccg ttggagactg cagcctccgc cgccgcttca gccgctgcag ccaccgcccg 3000 cgggattgtg actgactttg ctttcctgag cccgcttgca agcagtgcag cttcccgttc 3060 atccgcccgc gatgacaagt tgacggctct tttggcacaa ttggattctt tgacccggga 3120 acttaatgtc gtttctcagc agctgttgga tctgcgccag caggtttctg ccctgaaggc 3180 ttcctcccct cccaatgcgg tttaaaacat aaataaaaaa ccagactctg tttggatttg 3240 gatcaagcaa gtgtcttgct gtctttattt aggggttttg cgcgcgcggt aggcccggga 3300 ccagcggtct cggtcgttga gggtcctgtg tattttttcc aggacgtggt aaaggtgact 3360 ctggatgttc agatacatgg gcataagccc gtctctgggg tggaggtagc accactgcag 3420 agcttcatgc tgcggggtgg tgttgtagat gatccagtcg tagcaggagc gctgggcgtg 3480 gtgcctaaaa atgtctttca gtagcaagct gattgccagg ggcaggccct tggtgtaagt 3540 gtttacaaag cggttaagct gggatgggtg catacgtggg gatatgagat gcatcttgga 3600 ctgtattttt aggttggcta tgttcccagc catatccctc cggggattca tgttgtgcag 3660 aaccaccagc acagtgtatc cggtgcactt gggaaatttg tcatgtagct tagaaggaaa 3720 tgcgtggaag aacttggaga cgcccttgtg acctccaaga ttttccatgc attcgtccat 3780 aatgatggca atgggcccac gggcggcggc ctgggcgaag atatttctgg gatcactaac 3840 gtcatagttg tgttccagga tgagatcgtc ataggccatt tttacaaagc gcgggcggag 3900 ggtgccagac tgcggtataa tggttccatc cggcccaggg gcgtagttac cctcacagat 3960 ttgcatttcc cacgctttga gttcagatgg ggggatcatg tctacctgcg gggcgatgaa 4020 gaaaacggtt tccggggtag gggagatcag ctgggaagaa agcaggttcc tgagcagctg 4080 cgacttaccg cagccggtgg gcccgtaaat cacacctatt accgggtgca actggtagtt 4140 aagagagctg cagctgccgt catccctgag caggggggcc acttcgttaa gcatgtccct 4200 gactcgcatg ttttccctga ccaaatccgc cagaaggcgc tcgccgccca gcgatagcag 4260 ttcttgcaag gaagcaaagt ttttcaacgg tttgagaccg tccgccgtag gcatgctttt 4320 gagcgtttga ccaagcagtt ccaggcggtc ccacagctcg gtcacctgct ctacggcatc 4380 tcgatccagc atatctcctc gtttcgcggg ttggggcggc tttcgctgta cggcagtagt 4440 cggtgctcgt ccagacgggc cagggtcatg tctttccacg ggcgcagggt cctcgtcagc 4500 gtagtctggg tcacggtgaa ggggtgcgct ccgggctgcg cgctggccag ggtgcgcttg 4560 aggctggtcc tgctggtgct gaagcgctgc cggtcttcgc cctgcgcgtc ggccaggtag 4620 catttgacca tggtgtcata gtccagcccc tccgcggcgt ggcccttggc gcgcagcttg 4680 cccttggagg aggcgccgca cgaggggcag tgcagacttt tgagggcgta gagcttgggc 4740 gcgagaaata ccgattccgg ggagtaggca tccgcgccgc aggccccgca gacggtctcg 4800 cattccacga gccaggtgag ctctggccgt tcggggtcaa aaaccaggtt tcccccatgc 4860 tttttgatgc gtttcttacc tctggtttcc atgagccggt gtccacgctc ggtgacgaaa 4920 aggctgtccg tgtccccgta tacagacttg agaggcctgt cctcgagcgg tgttccgcgg 4980 tcctcctcgt atagaaactc ggaccactct gagacaaagg ctcgcgtcca ggccagcacg 5040 aaggaggcta agtgggaggg gtagcggtcg ttgtccacta gggggtccac tcgctccagg 5100 gtgtgaagac acatgtcgcc ctcttcggca tcaaggaagg tgattggttt gtaggtgtag 5160 gccacgtgac cgggtgttcc tgaagggggg ctataaaagg gggtgggggc gcgttcgtcc 5220 tcactctctt ccgcatcgct gtctgcgagg gccagctgtt ggggtgagta ctccctctga 5280 aaagcgggca tgacttctgc gctaagattg tcagtttcca aaaacgagga ggatttgata 5340 ttcacctggc ccgcggtgat gcctttgagg gtggccgcat ccatctggtc agaaaagaca 5400 atctttttgt tgtcaagctt ggtggcaaac gacccgtaga gggcgttgga cagcaacttg 5460 gcgatggagc gcagggtttg gtttttgtcg cgatcggcgc gctccttggc cgcgatgttt 5520 agctgcacgt attcgcgcgc aacgcaccgc cattcgggaa agacggtggt gcgctcgtcg 5580 ggcaccaggt gcacgcgcca accgcggttg tgcagggtga caaggtcaac gctggtggct 5640 acctctccgc gtaggcgctc gttggtccag cagaggcggc cgcccttgcg cgagcagaat 5700 ggcggtaggg ggtctagctg cgtctcgtcc ggggggtctg cgtccacggt aaagaccccg 5760 ggcagcaggc gcgcgtcgaa gtagtctatc ttgcatcctt gcaagtctag cgcctgctgc 5820 catgcgcggg cggcaagcgc gcgctcgtat gggttgagtg ggggacccca tggcatgggg 5880 tgggtgagcg cggaggcgta catgccgcaa atgtcgtaaa cgtagagggg ctctctgagt 5940 attccaagat atgtagggta gcatcttcca ccgcggatgc tggcgcgcac gtaatcgtat 6000 agttcgtgcg agggagcgag gaggtcggga ccgaggttgc tacgggcggg ctgctctgct 6060 cggaagacta tctgcctgaa gatggcatgt gagttggatg atatggttgg acgctggaag 6120 acgttgaagc tggcgtctgt gagacctacc gcgtcacgca cgaaggaggc gtaggagtcg 6180 cgcagcttgt tgaccagctc ggcggtgacc tgcacgtcta gggcgcagta gtccagggtt 6240 tccttgatga tgtcatactt atcctgtccc ttttttttcc acagctcgcg gttgaggaca 6300 aactcttcgc ggtctttcca gtactcttgg atcggaaacc cgtcggcctc cgaacggtaa 6360 gagcctagca tgtagaactg gttgacggcc tggtaggcgc agcatccctt ttctacgggt 6420 agcgcgtatg cctgcgcggc cttccggagc gaggtgtggg tgagcgcaaa ggtgtccctg 6480 accatgactt tgaggtactg gtatttgaag tcagtgtcgt cgcatccgcc ctgctcccag 6540 agcaaaaagt ccgtgcgctt tttggaacgc ggatttggca gggcgaaggt gacatcgttg 6600 aagagtatct ttcccgcgcg aggcataaag ttgcgtgtga tgcggaaggg tcccggcacc 6660 tcggaacggt tgttaattac ctgggcggcg agcacgatct cgtcaaagcc gttgatgttg 6720 tggcccacaa tgtaaagttc caagaagcgc gggatgccct tgatggaagg caatttttta 6780 agttcctcgt aggtgagctc ttcaggggag ctgagcccgt gctctgaaag ggcccagtct 6840 gcaagatgag ggttggaagc gacgaatgag ctccacaggt cacgggccat tagcatttgc 6900 aggtggtcgc gaaaggtcct aaactggcga cctatggcca ttttttctgg ggtgatgcag 6960 tagaaggtaa gcgggtcttg ttcccagcgg tcccatccaa ggttcgcggc taggtctcgc 7020 gcggcagtca ctagaggctc atctccgccg aacttcatga ccagcatgaa gggcacgagc 7080 tgcttcccaa aggcccccat ccaagtatag gtctctacat cgtaggtgac aaagagacgc 7140 tcggtgcgag gatgcgagcc gatcgggaag aactggatct cccgccacca attggaggag 7200 tggctattga tgtggtgaaa gtagaagtcc ctgcgacggg ccgaacactc gtgctggctt 7260 ttgtaaaaac gtgcgcagta ctggcagcgg tgcacgggct gtacatcctg cacgaggttg 7320 acctgacgac cgcgcacaag gaagcagagt gggaatttga gcccctcgcc tggcgggttt 7380 ggctggtggt cttctacttc ggctgcttgt ccttgaccgt ctggctgctc gaggggagtt 7440 acggtggatc ggaccaccac gccgcgcgag cccaaagtcc agatgtccgc gcgcggcggt 7500 cggagcttga tgacaacatc gcgcagatgg gagctgtcca tggtctggag ctcccgcggc 7560 gtcaggtcag gcgggagctc ctgcaggttt acctcgcata gacgggtcag ggcgcgggct 7620 agatccaggt gatacctaat ttccaggggc tggttggtgg cggcgtcgat ggcttgcaag 7680 aggccgcatc cccgcggcgc gactacggta ccgcgcggcg ggcggtgggc cgcgggggtg 7740 tccttggatg atgcatctaa aagcggtgac gcgggcgagc ccccggaggt agggggggct 7800 ccggacccgc cgggagaggg ggcaggggca cgtcggcgcc gcgcgcgggc aggagctggt 7860 gctgcgcgcg taggttgctg gcgaacgcga cgacgcggcg gttgatctcc tgaatctggc 7920 gcctctgcgt gaagacgacg ggcccggtga gcttgagcct gaaagagagt tcgacagaat 7980 caatttcggt gtcgttgacg gcggcctggc gcaaaatctc ctgcacgtct cctgagttgt 8040 cttgataggc gatctcggcc atgaactgct cgatctcttc ctcctggaga tctccgcgtc 8100 cggctcgctc cacggtggcg gcgaggtcgt tggaaatgcg ggccatgagc tgcgagaagg 8160 cgttgaggcc tccctcgttc cagacgcggc tgtagaccac gcccccttcg gcatcgcggg 8220 cgcgcatgac cacctgcgcg agattgagct ccacgtgccg ggcgaagacg gcgtagtttc 8280 gcaggcgctg aaagaggtag ttgagggtgg tggcggtgtg ttctgccacg aagaagtaca 8340 taacccagcg tcgcaacgtg gattcgttga tatcccccaa ggcctcaagg cgctccatgg 8400 cctcgtagaa gtccacggcg aagttgaaaa actgggagtt gcgcgccgac acggttaact 8460 cctcctccag aagacggatg agctcggcga cagtgtcgcg cacctcgcgc tcaaaggcta 8520 caggggcctc ttcttcttct tcaatctcct cttccataag ggcctcccct tcttcttctt 8580 ctggcggcgg tgggggaggg gggacacggc ggcgacgacg gcgcaccggg aggcggtcga 8640 caaagcgctc gatcatctcc ccgcggcgac ggcgcatggt ctcggtgacg gcgcggccgt 8700 tctcgcgggg gcgcagttgg aagacgccgc ccgtcatgtc ccggttatgg gttggcgggg 8760 ggctgccatg cggcagggat acggcgctaa cgatgcatct caacaattgt tgtgtaggta 8820 ctccgccgcc gagggacctg agcgagtccg catcgaccgg atcggaaaac ctctcgagaa 8880 aggcgtctaa ccagtcacag tcgcaaggta ggctgagcac cgtggcgggc ggcagcgggc 8940 ggcggtcggg gttgtttctg gcggaggtgc tgctgatgat gtaattaaag taggcggtct 9000 tgagacggcg gatggtcgac agaagcacca tgtccttggg tccggcctgc tgaatgcgca 9060 ggcggtcggc catgccccag gcttcgtttt gacatcggcg caggtctttg tagtagtctt 9120 gcatgagcct ttctaccggc acttcttctt ctccttcctc ttgtcctgca tctcttgcat 9180 ctatcgctgc ggcggcggcg gagtttggcc gtaggtggcg ccctcttcct cccatgcgtg 9240 tgaccccgaa gcccctcatc ggctgaagca gggctaggtc ggcgacaacg cgctcggcta 9300 atatggcctg ctgcacctgc gtgagggtag actggaagtc atccatgtcc acaaagcggt 9360 ggtatgcgcc cgtgttgatg gtgtaagtgc agttggccat aacggaccag ttaacggtct 9420 ggtgacccgg ctgcgagagc tcggtgtacc tgagacgcga gtaagccctc gagtcaaata 9480 cgtagtcgtt gcaagtccgc accaggtact ggtatcccac caaaaagtgc ggcggcggct 9540 ggcggtagag gggccagcgt agggtggccg gggctccggg ggcgagatct tccaacataa 9600 ggcgatgata tccgtagatg tacctggaca tccaggtgat gccggcggcg gtggtggagg 9660 cgcgcggaaa gtcgcggacg cggttccaga tgttgcgcag cggcaaaaag tgctccatgg 9720 tcgggacgct ctggccggtc aggcgcgcgc aatcgttgac gctctagacc gtgcaaaagg 9780 agagcctgta agcgggcact cttccgtggt ctggtggata aattcgcaag ggtatcatgg 9840 cggacgaccg gggttcgagc cccgtatccg gccgtccgcc gtgatccatg cggttaccgc 9900 ccgcgtgtcg aacccaggtg tgcgacgtca gacaacgggg gagtgctcct tttggcttcc 9960 ttccaggcgc ggcggctgct gcgctagctt ttttggccac tggccgcgcg cagcgtaagc 10020 ggttaggctg gaaagcgaaa gcattaagtg gctcgctccc tgtagccgga gggttatttt 10080 ccaagggttg agtcgcggga cccccggttc gagtctcgga ccggccggac tgcggcgaac 10140 gggggtttgc ctccccgtca tgcaagaccc cgcttgcaaa ttcctccgga aacagggacg 10200 agcccctttt ttgcttttcc cagatgcatc cggtgctgcg gcagatgcgc ccccctcctc 10260 agcagcggca agagcaagag cagcggcaga catgcagggc accctcccct cctcctaccg 10320 cgtcaggagg ggcgacatcc gcggttgacg cggcagcaga tggtgattac gaacccccgc 10380 ggcgccgggc ccggcactac ctggacttgg aggagggcga gggcctggcg cggctaggag 10440 cgccctctcc tgagcggtac ccaagggtgc agctgaagcg tgatacgcgt gaggcgtacg 10500 tgccgcggca gaacctgttt cgcgaccgcg agggagagga gcccgaggag atgcgggatc 10560 gaaagttcca cgcagggcgc gagctgcggc atggcctgaa tcgcgagcgg ttgctgcgcg 10620 aggaggactt tgagcccgac gcgcgaaccg ggattagtcc cgcgcgcgca cacgtggcgg 10680 ccgccgacct ggtaaccgca tacgagcaga cggtgaacca ggagattaac tttcaaaaaa 10740 gctttaacaa ccacgtgcgt acgcttgtgg cgcgcgagga ggtggctata ggactgatgc 10800 atctgtggga ctttgtaagc gcgctggagc aaaacccaaa tagcaagccg ctcatggcgc 10860 agctgttcct tatagtgcag cacagcaggg acaacgaggc attcagggat gcgctgctaa 10920 acatagtaga gcccgagggc cgctggctgc tcgatttgat aaacatcctg cagagcatag 10980 tggtgcagga gcgcagcttg agcctggctg acaaggtggc cgccatcaac tattccatgc 11040 ttagcctggg caagttttac gcccgcaaga tataccatac cccttacgtt cccatagaca 11100 aggaggtaaa gatcgagggg ttctacatgc gcatggcgct gaaggtgctt accttgagcg 11160 acgacctggg cgtttatcgc aacgagcgca tccacaaggc cgtgagcgtg agccggcggc 11220 gcgagctcag cgaccgcgag ctgatgcaca gcctgcaaag ggccctggct ggcacgggca 11280 gcggcgatag agaggccgag tcctactttg acgcgggcgc tgacctgcgc tgggccccaa 11340 gccgacgcgc cctggaggca gctggggccg gacctgggct ggcggtggca cccgcgcgcg 11400 ctggcaacgt cggcggcgtg gaggaatatg acgaggacga tgagtacgag ccagaggacg 11460 gcgagtacta agcggtgatg tttctgatca gatgatgcaa gacgcaacgg acccggcggt 11520 gcgggcggcg ctgcagagcc agccgtccgg ccttaactcc acggacgact ggcgccaggt 11580 catggaccgc atcatgtcgc tgactgcgcg caatcctgac gcgttccggc agcagccgca 11640 ggccaaccgg ctctccgcaa ttctggaagc ggtggtcccg gcgcgcgcaa accccacgca 11700 cgagaaggtg ctggcgatcg taaacgcgct ggccgaaaac agggccatcc ggcccgacga 11760 ggccggcctg gtctacgacg cgctgcttca gcgcgtggct cgttacaaca gcggcaacgt 11820 gcagaccaac ctggaccggc tggtggggga tgtgcgcgag gccgtggcgc agcgtgagcg 11880 cgcgcagcag cagggcaacc tgggctccat ggttgcacta aacgccttcc tgagtacaca 11940 gcccgccaac gtgccgcggg gacaggagga ctacaccaac tttgtgagcg cactgcggct 12000 aatggtgact gagacaccgc aaagtgaggt gtaccagtct gggccagact attttttcca 12060 gaccagtaga caaggcctgc agaccgtaaa cctgagccag gctttcaaaa acttgcaggg 12120 gctgtggggg gtgcgggctc ccacaggcga ccgcgcgacc gtgtctagct tgctgacgcc 12180 caactcgcgc ctgttgctgc tgctaatagc gcccttcacg gacagtggca gcgtgtcccg 12240 ggacacatac ctaggtcact tgctgacact gtaccgcgag gccataggtc aggcgcatgt 12300 ggacgagcat actttccagg agattacaag tgtcagccgc gcgctggggc aggaggacac 12360 gggcagcctg gaggcaaccc taaactacct gctgaccaac cggcggcaga agatcccctc 12420 gttgcacagt ttaaacagcg aggaggagcg cattttgcgc tacgtgcagc agagcgtgag 12480 ccttaacctg atgcgcgacg gggtaacgcc cagcgtggcg ctggacatga ccgcgcgcaa 12540 catggaaccg ggcatgtatg cctcaaaccg gccgtttatc aaccgcctaa tggactactt 12600 gcatcgcgcg gccgccgtga accccgagta tttcaccaat gccatcttga acccgcactg 12660 gctaccgccc cctggtttct acaccggggg attcgaggtg cccgagggta acgatggatt 12720 cctctgggac gacatagacg acagcgtgtt ttccccgcaa ccgcagaccc tgctagagtt 12780 gcaacagcgc gagcaggcag aggcggcgct gcgaaaggaa agcttccgca ggccaagcag 12840 cttgtccgat ctaggcgctg cggccccgcg gtcagatgct agtagcccat ttccaagctt 12900 gatagggtct cttaccagca ctcgcaccac ccgcccgcgc ctgctgggcg aggaggagta 12960 cctaaacaac tcgctgctgc agccgcagcg cgaaaaaaac ctgcctccgg catttcccaa 13020 caacgggata gagagcctag tggacaagat gagtagatgg aagacgtacg cgcaggagca 13080 cagggacgtg ccaggcccgc gcccgcccac ccgtcgtcaa aggcacgacc gtcagcgggg 13140 tctggtgtgg gaggacgatg actcggcaga cgacagcagc gtcctggatt tgggagggag 13200 tggcaacccg tttgcgcacc ttcgccccag gctggggaga atgttttaaa aaaaaaaaag 13260 catgatgcaa aataaaaaac tcaccaaggc catggcaccg agcgttggtt ttcttgtatt 13320 ccccttagta tgcggcgcgc ggcgatgtat gaggaaggtc ctcctccctc ctacgagagt 13380 gtggtgagcg cggcgccagt ggcggcggcg ctgggttctc ccttcgatgc tcccctggac 13440 ccgccgtttg tgcctccgcg gtacctgcgg cctaccgggg ggagaaacag catccgttac 13500 tctgagttgg cacccctatt cgacaccacc cgtgtgtacc tggtggacaa caagtcaacg 13560 gatgtggcat ccctgaacta ccagaacgac cacagcaact ttctgaccac ggtcattcaa 13620 aacaatgact acagcccggg ggaggcaagc acacagacca tcaatcttga cgaccggtcg 13680 cactggggcg gcgacctgaa aaccatcctg cataccaaca tgccaaatgt gaacgagttc 13740 atgtttacca ataagtttaa ggcgcgggtg atggtgtcgc gcttgcctac taaggacaat 13800 caggtggagc tgaaatacga gtgggtggag ttcacgctgc ccgagggcaa ctactccgag 13860 accatgacca tagaccttat gaacaacgcg atcgtggagc actacttgaa agtgggcaga 13920 cagaacgggg ttctggaaag cgacatcggg gtaaagtttg acacccgcaa cttcagactg 13980 gggtttgacc ccgtcactgg tcttgtcatg cctggggtat atacaaacga agccttccat 14040 ccagacatca ttttgctgcc aggatgcggg gtggacttca cccacagccg cctgagcaac 14100 ttgttgggca tccgcaagcg gcaacccttc caggagggct ttaggatcac ctacgatgat 14160 ctggagggtg gtaacattcc cgcactgttg gatgtggacg cctaccaggc gagcttgaaa 14220 gatgacaccg aacagggcgg gggtggcgca ggcggcagca acagcagtgg cagcggcgcg 14280 gaagagaact ccaacgcggc agccgcggca atgcagccgg tggaggacat gaacgatcat 14340 gccattcgcg gcgacacctt tgccacacgg gctgaggaga agcgcgctga ggccgaagca 14400 gcggccgaag ctgccgcccc cgctgcgcaa cccgaggtcg agaagcctca gaagaaaccg 14460 gtgatcaaac ccctgacaga ggacagcaag aaacgcagtt acaacctaat aagcaatgac 14520 agcaccttca cccagtaccg cagctggtac cttgcataca actacggcga ccctcagacc 14580 ggaatccgct catggaccct gctttgcact cctgacgtaa cctgcggctc ggagcaggtc 14640 tactggtcgt tgccagacat gatgcaagac cccgtgacct tccgctccac gcgccagatc 14700 agcaactttc cggtggtggg cgccgagctg ttgcccgtgc actccaagag cttctacaac 14760 gaccaggccg tctactccca actcatccgc cagtttacct ctctgaccca cgtgttcaat 14820 cgctttcccg agaaccagat tttggcgcgc ccgccagccc ccaccatcac caccgtcagt 14880 gaaaacgttc ctgctctcac agatcacggg acgctaccgc tgcgcaacag catcggagga 14940 gtccagcgag tgaccattac tgacgccaga cgccgcacct gcccctacgt ttacaaggcc 15000 ctgggcatag tctcgccgcg cgtcctatcg agccgcactt tttgagcaag catgtccatc 15060 cttatatcgc ccagcaataa cacaggctgg ggcctgcgct tcccaagcaa gatgtttggc 15120 ggggccaaga agcgctccga ccaacaccca gtgcgcgtgc gcgggcacta ccgcgcgccc 15180 tggggcgcgc acaaacgcgg ccgcactggg cgcaccaccg tcgatgacgc catcgacgcg 15240 gtggtggagg aggcgcgcaa ctacacgccc acgccgccac cagtgtccac agtggacgcg 15300 gccattcaga ccgtggtgcg cggagcccgg cgctatgcta aaatgaagag acggcggagg 15360 cgcgtagcac gtcgccaccg ccgccgaccc ggcactgccg cccaacgcgc ggcggcggcc 15420 ctgcttaacc gcgcacgtcg caccggccga cgggcggcca tgcgggccgc tcgaaggctg 15480 gccgcgggta ttgtcactgt gccccccagg tccaggcgac gagcggccgc cgcagcagcc 15540 gcggccatta gtgctatgac tcagggtcgc aggggcaacg tgtattgggt gcgcgactcg 15600 gttagcggcc tgcgcgtgcc cgtgcgcacc cgccccccgc gcaactagat tgcaagaaaa 15660 aactacttag actcgtactg ttgtatgtat ccagcggcgg cggcgcgcaa cgaagctatg 15720 tccaagcgca aaatcaaaga agagatgctc caggtcatcg cgccggagat ctatggcccc 15780 ccgaagaagg aagagcagga ttacaagccc cgaaagctaa agcgggtcaa aaagaaaaag 15840 aaagatgatg atgatgaact tgacgacgag gtggaactgc tgcacgctac cgcgcccagg 15900 cgacgggtac agtggaaagg tcgacgcgta aaacgtgttt tgcgacccgg caccaccgta 15960 gtctttacgc ccggtgagcg ctccacccgc acctacaagc gcgtgtatga tgaggtgtac 16020 ggcgacgagg acctgcttga gcaggccaac gagcgcctcg gggagtttgc ctacggaaag 16080 cggcataagg acatgctggc gttgccgctg gacgagggca acccaacacc tagcctaaag 16140 cccgtaacac tgcagcaggt gctgcccgcg cttgcaccgt ccgaagaaaa gcgcggccta 16200 aagcgcgagt ctggtgactt ggcacccacc gtgcagctga tggtacccaa gcgccagcga 16260 ctggaagatg tcttggaaaa aatgaccgtg gaacctgggc tggagcccga ggtccgcgtg 16320 cggccaatca agcaggtggc gccgggactg ggcgtgcaga ccgtggacgt tcagataccc 16380 actaccagta gcaccagtat tgccaccgcc acagagggca tggagacaca aacgtccccg 16440 gttgcctcag cggtggcgga tgccgcggtg caggcggtcg ctgcggccgc gtccaagacc 16500 tctacggagg tgcaaacgga cccgtggatg tttcgcgttt cagccccccg gcgcccgcgc 16560 ggttcgagga agtacggcgc cgccagcgcg ctactgcccg aatatgccct acatccttcc 16620 attgcgccta cccccggcta tcgtggctac acctaccgcc ccagaagacg agcaactacc 16680 cgacgccgaa ccaccactgg aacccgccgc cgccgtcgcc gtcgccagcc cgtgctggcc 16740 ccgatttccg tgcgcagggt ggctcgcgaa ggaggcagga ccctggtgct gccaacagcg 16800 cgctaccacc ccagcatcgt ttaaaagccg gtctttgtgg ttcttgcaga tatggccctc 16860 acctgccgcc tccgtttccc ggtgccggga ttccgaggaa gaatgcaccg taggaggggc 16920 atggccggcc acggcctgac gggcggcatg cgtcgtgcgc accaccggcg gcggcgcgcg 16980 tcgcaccgtc gcatgcgcgg cggtatcctg cccctcctta ttccactgat cgccgcggcg 17040 attggcgccg tgcccggaat tgcatccgtg gccttgcagg cgcagagaca ctgattaaaa 17100 acaagttgca tgtggaaaaa tcaaaataaa aagtctggac tctcacgctc gcttggtcct 17160 gtaactattt tgtagaatgg aagacatcaa ctttgcgtct ctggccccgc gacacggctc 17220 gcgcccgttc atgggaaact ggcaagatat cggcaccagc aatatgagcg gtggcgcctt 17280 cagctggggc tcgctgtgga gcggcattaa aaatttcggt tccaccgtta agaactatgg 17340 cagcaaggcc tggaacagca gcacaggcca gatgctgagg gataagttga aagagcaaaa 17400 tttccaacaa aaggtggtag atggcctggc ctctggcatt agcggggtgg tggacctggc 17460 caaccaggca gtgcaaaata agattaacag taagcttgat ccccgccctc ccgtagagga 17520 gcctccaccg gccgtggaga cagtgtctcc agaggggcgt ggcgaaaagc gtccgcgccc 17580 cgacagggaa gaaactctgg tgacgcaaat agacgagcct ccctcgtacg aggaggcact 17640 aaagcaaggc ctgcccacca cccgtcccat cgcgcccatg gctaccggag tgctgggcca 17700 gcacacaccc gtaacgctgg acctgcctcc ccccgccgac acccagcaga aacctgtgct 17760 gccaggcccg accgccgttg ttgtaacccg tcctagccgc gcgtccctgc gccgcgccgc 17820 cagcggtccg cgatcgttgc ggcccgtagc cagtggcaac tggcaaagca cactgaacag 17880 catcgtgggt ctgggggtgc aatccctgaa gcgccgacga tgcttctgaa tagctaacgt 17940 gtcgtatgtg tgtcatgtat gcgtccatgt cgccgccaga ggagctgctg agccgccgcg 18000 cgcccgcttt ccaagatggc taccccttcg atgatgccgc agtggtctta catgcacatc 18060 tcgggccagg acgcctcgga gtacctgagc cccgggctgg tgcagtttgc ccgcgccacc 18120 gagacgtact tcagcctgaa taacaagttt agaaacccca cggtggcgcc tacgcacgac 18180 gtgaccacag accggtccca gcgtttgacg ctgcggttca tccctgtgga ccgtgaggat 18240 actgcgtact cgtacaaggc gcggttcacc ctagctgtgg gtgataaccg tgtgctggac 18300 atggcttcca cgtactttga catccgcggc gtgctggaca ggggccctac ttttaagccc 18360 tactctggca ctgcctacaa cgccctggct cccaagggtg ccccaaatcc ttgcgaatgg 18420 gatgaagctg ctactgctct tgaaataaac ctagaagaag aggacgatga caacgaagac 18480 gaagtagacg agcaagctga gcagcaaaaa actcacgtat ttgggcaggc gccttattct 18540 ggtataaata ttacaaagga gggtattcaa ataggtgtcg aaggtcaaac acctaaatat 18600 gccgataaaa catttcaacc tgaacctcaa ataggagaat ctcagtggta cgaaactgaa 18660 attaatcatg cagctgggag agtccttaaa aagactaccc caatgaaacc atgttacggt 18720 tcatatgcaa aacccacaaa tgaaaatgga gggcaaggca ttcttgtaaa gcaacaaaat 18780 ggaaagctag aaagtcaagt ggaaatgcaa tttttctcaa ctactgaggc gaccgcaggc 18840 aatggtgata acttgactcc taaagtggta ttgtacagtg aagatgtaga tatagaaacc 18900 ccagacactc atatttctta catgcccact attaaggaag gtaactcacg agaactaatg 18960 ggccaacaat ctatgcccaa caggcctaat tacattgctt ttagggacaa ttttattggt 19020 ctaatgtatt acaacagcac gggtaatatg ggtgttctgg cgggccaagc atcgcagttg 19080 aatgctgttg tagatttgca agacagaaac acagagcttt cataccagct tttgcttgat 19140 tccattggtg atagaaccag gtacttttct atgtggaatc aggctgttga cagctatgat 19200 ccagatgtta gaattattga aaatcatgga actgaagatg aacttccaaa ttactgcttt 19260 ccactgggag gtgtgattaa tacagagact cttaccaagg taaaacctaa aacaggtcag 19320 gaaaatggat gggaaaaaga tgctacagaa ttttcagata aaaatgaaat aagagttgga 19380 aataattttg ccatggaaat caatctaaat gccaacctgt ggagaaattt cctgtactcc 19440 aacatagcgc tgtatttgcc cgacaagcta aagtacagtc cttccaacgt aaaaatttct 19500 gataacccaa acacctacga ctacatgaac aagcgagtgg tggctcccgg gttagtggac 19560 tgctacatta accttggagc acgctggtcc cttgactata tggacaacgt caacccattt 19620 aaccaccacc gcaatgctgg cctgcgctac cgctcaatgt tgctgggcaa tggtcgctat 19680 gtgcccttcc acatccaggt gcctcagaag ttctttgcca ttaaaaacct ccttctcctg 19740 ccgggctcat acacctacga gtggaacttc aggaaggatg ttaacatggt tctgcagagc 19800 tccctaggaa atgacctaag ggttgacgga gccagcatta agtttgatag catttgcctt 19860 tacgccacct tcttccccat ggcccacaac accgcctcca cgcttgaggc catgcttaga 19920 aacgacacca acgaccagtc ctttaacgac tatctctccg ccgccaacat gctctaccct 19980 atacccgcca acgctaccaa cgtgcccata tccatcccct cccgcaactg ggcggctttc 20040 cgcggctggg ccttcacgcg ccttaagact aaggaaaccc catcactggg ctcgggctac 20100 gacccttatt acacctactc tggctctata ccctacctag atggaacctt ttacctcaac 20160 cacaccttta agaaggtggc cattaccttt gactcttctg tcagctggcc tggcaatgac 20220 cgcctgctta cccccaacga gtttgaaatt aagcgctcag ttgacgggga gggttacaac 20280 gttgcccagt gtaacatgac caaagactgg ttcctggtac aaatgctagc taactacaac 20340 attggctacc agggcttcta tatcccagag agctacaagg accgcatgta ctccttcttt 20400 agaaacttcc agcccatgag ccgtcaggtg gtggatgata ctaaatacaa ggactaccaa 20460 caggtgggca tcctacacca acacaacaac tctggatttg ttggctacct tgcccccacc 20520 atgcgcgaag gacaggccta ccctgctaac ttcccctatc cgcttatagg caagaccgca 20580 gttgacagca ttacccagaa aaagtttctt tgcgatcgca ccctttggcg catcccattc 20640 tccagtaact ttatgtccat gggcgcactc acagacctgg gccaaaacct tctctacgcc 20700 aactccgccc acgcgctaga catgactttt gaggtggatc ccatggacga gcccaccctt 20760 ctttatgttt tgtttgaagt ctttgacgtg gtccgtgtgc accggccgca ccgcggcgtc 20820 atcgaaaccg tgtacctgcg cacgcccttc tcggccggca acgccacaac ataaagaagc 20880 aagcaacatc aacaacagct gccgccatgg gctccagtga gcaggaactg aaagccattg 20940 tcaaagatct tggttgtggg ccatattttt tgggcaccta tgacaagcgc tttccaggct 21000 ttgtttctcc acacaagctc gcctgcgcca tagtcaatac ggccggtcgc gagactgggg 21060 gcgtacactg gatggccttt gcctggaacc cgcactcaaa aacatgctac ctctttgagc 21120 cctttggctt ttctgaccag cgactcaagc aggtttacca gtttgagtac gagtcactcc 21180 tgcgccgtag cgccattgct tcttcccccg accgctgtat aacgctggaa aagtccaccc 21240 aaagcgtaca ggggcccaac tcggccgcct gtggactatt ctgctgcatg tttctccacg 21300 cctttgccaa ctggccccaa actcccatgg atcacaaccc caccatgaac cttattaccg 21360 gggtacccaa ctccatgctc aacagtcccc aggtacagcc caccctgcgt cgcaaccagg 21420 aacagctcta cagcttcctg gagcgccact cgccctactt ccgcagccac agtgcgcaga 21480 ttaggagcgc cacttctttt tgtcacttga aaaacatgta aaaataatgt actagagaca 21540 ctttcaataa aggcaaatgc ttttatttgt acactctcgg gtgattattt acccccaccc 21600 ttgccgtctg cgccgtttaa aaatcaaagg ggttctgccg cgcatcgcta tgcgccactg 21660 gcagggacac gttgcgatac tggtgtttag tgctccactt aaactcaggc acaaccatcc 21720 gcggcagctc ggtgaagttt tcactccaca ggctgcgcac catcaccaac gcgtttagca 21780 ggtcgggcgc cgatatcttg aagtcgcagt tggggcctcc gccctgcgcg cgcgagttgc 21840 gatacacagg gttgcagcac tggaacacta tcagcgccgg gtggtgcacg ctggccagca 21900 cgctcttgtc ggagatcaga tccgcgtcca ggtcctccgc gttgctcagg gcgaacggag 21960 tcaactttgg tagctgcctt cccaaaaagg gcgcgtgccc aggctttgag ttgcactcgc 22020 accgtagtgg catcaaaagg tgaccgtgcc cggtctgggc gttaggatac agcgcctgca 22080 taaaagcctt gatctgctta aaagccacct gagcctttgc gccttcagag aagaacatgc 22140 cgcaagactt gccggaaaac tgattggccg gacaggccgc gtcgtgcacg cagcaccttg 22200 cgtcggtgtt ggagatctgc accacatttc ggccccaccg gttcttcacg atcttggcct 22260 tgctagactg ctccttcagc gcgcgctgcc cgttttcgct cgtcacatcc atttcaatca 22320 cgtgctcctt atttatcata atgcttccgt gtagacactt aagctcgcct tcgatctcag 22380 cgcagcggtg cagccacaac gcgcagcccg tgggctcgtg atgcttgtag gtcacctctg 22440 caaacgactg caggtacgcc tgcaggaatc gccccatcat cgtcacaaag gtcttgttgc 22500 tggtgaaggt cagctgcaac ccgcggtgct cctcgttcag ccaggtcttg catacggccg 22560 ccagagcttc cacttggtca ggcagtagtt tgaagttcgc ctttagatcg ttatccacgt 22620 ggtacttgtc catcagcgcg cgcgcagcct ccatgccctt ctcccacgca gacacgatcg 22680 gcacactcag cgggttcatc accgtaattt cactttccgc ttcgctgggc tcttcctctt 22740 cctcttgcgt ccgcatacca cgcgccactg ggtcgtcttc attcagccgc cgcactgtgc 22800 gcttacctcc tttgccatgc ttgattagca ccggtgggtt gctgaaaccc accatttgta 22860 gcgccacatc ttctctttct tcctcgctgt ccacgattac ctctggtgat ggcgggcgct 22920 cgggcttggg agaagggcgc ttctttttct tcttgggcgc aatggccaaa tccgccgccg 22980 aggtcgatgg ccgcgggctg ggtgtgcgcg gcaccagcgc gtcttgtgat gagtcttcct 23040 cgtcctcgga ctcgatacgc cgcctcatcc gcttttttgg gggcgcccgg ggaggcggcg 23100 gcgacgggga cggggacgac acgtcctcca tggttggggg acgtcgcgcc gcaccgcgtc 23160 cgcgctcggg ggtggtttcg cgctgctcct cttcccgact ggccatttcc ttctcctata 23220 ggcagaaaaa gatcatggag tcagtcgaga agaaggacag cctaaccgcc ccctctgagt 23280 tcgccaccac cgcctccacc gatgccgcca acgcgcctac caccttcccc gtcgaggcac 23340 ccccgcttga ggaggaggaa gtgattatcg agcaggaccc aggttttgta agcgaagacg 23400 acgaggaccg ctcagtacca acagaggata aaaagcaaga ccaggacaac gcagaggcaa 23460 acgaggaaca agtcgggcgg ggggacgaaa ggcatggcga ctacctagat gtgggagacg 23520 acgtgctgtt gaagcatctg cagcgccagt gcgccattat ctgcgacgcg ttgcaagagc 23580 gcagcgatgt gcccctcgcc atagcggatg tcagccttgc ctacgaacgc cacctattct 23640 caccgcgcgt accccccaaa cgccaagaaa acggcacatg cgagcccaac ccgcgcctca 23700 acttctaccc cgtatttgcc gtgccagagg tgcttgccac ctatcacatc tttttccaaa 23760 actgcaagat acccctatcc tgccgtgcca accgcagccg agcggacaag cagctggcct 23820 tgcggcaggg cgctgtcata cctgatatcg cctcgctcaa cgaagtgcca aaaatctttg 23880 agggtcttgg acgcgacgag aagcgcgcgg caaacgctct gcaacaggaa aacagcgaaa 23940 atgaaagtca ctctggagtg ttggtggaac tcgagggtga caacgcgcgc ctagccgtac 24000 taaaacgcag catcgaggtc acccactttg cctacccggc acttaaccta ccccccaagg 24060 tcatgagcac agtcatgagt gagctgatcg tgcgccgtgc gcagcccctg gagagggatg 24120 caaatttgca agaacaaaca gaggagggcc tacccgcagt tggcgacgag cagctagcgc 24180 gctggcttca aacgcgcgag cctgccgact tggaggagcg acgcaaacta atgatggccg 24240 cagtgctcgt taccgtggag cttgagtgca tgcagcggtt ctttgctgac ccggagatgc 24300 agcgcaagct agaggaaaca ttgcactaca cctttcgaca gggctacgta cgccaggcct 24360 gcaagatctc caacgtggag ctctgcaacc tggtctccta ccttggaatt ttgcacgaaa 24420 accgccttgg gcaaaacgtg cttcattcca cgctcaaggg cgaggcgcgc cgcgactacg 24480 tccgcgactg cgtttactta tttctatgct acacctggca gacggccatg ggcgtttggc 24540 agcagtgctt ggaggagtgc aacctcaagg agctgcagaa actgctaaag caaaacttga 24600 aggacctatg gacggccttc aacgagcgct ccgtggccgc gcacctggcg gacatcattt 24660 tccccgaacg cctgcttaaa accctgcaac agggtctgcc agacttcacc agtcaaagca 24720 tgttgcagaa ctttaggaac tttatcctag agcgctcagg aatcttgccc gccacctgct 24780 gtgcacttcc tagcgacttt gtgcccatta agtaccgcga atgccctccg ccgctttggg 24840 gccactgcta ccttctgcag ctagccaact accttgccta ccactctgac ataatggaag 24900 acgtgagcgg tgacggtcta ctggagtgtc actgtcgctg caacctatgc accccgcacc 24960 gctccctggt ttgcaattcg cagctgctta acgaaagtca aattatcggt acctttgagc 25020 tgcagggtcc ctcgcctgac gaaaagtccg cggctccggg gttgaaactc actccggggc 25080 tgtggacgtc ggcttacctt cgcaaatttg tacctgagga ctaccacgcc cacgagatta 25140 ggttctacga agaccaatcc cgcccgccaa atgcggagct taccgcctgc gtcattaccc 25200 agggccacat tcttggccaa ttgcaagcca tcaacaaagc ccgccaagag tttctgctac 25260 gaaagggacg gggggtttac ttggaccccc agtccggcga ggagctcaac ccaatccccc 25320 cgccgccgca gccctatcag cagcagccgc gggcccttgc ttcccaggat ggcacccaaa 25380 aagaagctgc agctgccgcc gccacccacg gacgaggagg aatactggga cagtcaggca 25440 gaggaggttt tggacgagga ggaggaggac atgatggaag actgggagag cctagacgag 25500 gaagcttccg aggtcgaaga ggtgtcagac gaaacaccgt caccctcggt cgcattcccc 25560 tcgccggcgc cccagaaatc ggcaaccggt tccagcatgg ctacaacctc cgctcctcag 25620 gcgccgccgg cactgcccgt tcgccgaccc aaccgtagat gggacaccac tggaaccagg 25680 gccggtaagt ccaagcagcc gccgccgtta gcccaagagc aacaacagcg ccaaggctac 25740 cgctcatggc gcgggcacaa gaacgccata gttgcttgct tgcaagactg tgggggcaac 25800 atctccttcg cccgccgctt tcttctctac catcacggcg tggccttccc ccgtaacatc 25860 ctgcattact accgtcatct ctacagccca tactgcaccg gcggcagcgg cagcggcagc 25920 aacagcagcg gccacacaga agcaaaggcg accggatagc aagactctga caaagcccaa 25980 gaaatccaca gcggcggcag cagcaggagg aggagcgctg cgtctggcgc ccaacgaacc 26040 cgtatcgacc cgcgagctta gaaacaggat ttttcccact ctgtatgcta tatttcaaca 26100 gagcaggggc caagaacaag agctgaaaat aaaaaacagg tctctgcgat ccctcacccg 26160 cagctgcctg tatcacaaaa gcgaagatca gcttcggcgc acgctggaag acgcggaggc 26220 tctcttcagt aaatactgcg cgctgactct taaggactag tttcgcgccc tttctcaaat 26280 ttaagcgcga aaactacgtc atctccagcg gccacacccg gcgccagcac ctgtcgtcag 26340 cgccattatg agcaaggaaa ttcccacgcc ctacatgtgg agttaccagc cacaaatggg 26400 acttgcggct ggagctgccc aagactactc aacccgaata aactacatga gcgcgggacc 26460 ccacatgata tcccgggtca acggaatccg cgcccaccga aaccgaattc tcttggaaca 26520 ggcggctatt accaccacac ctcgtaataa ccttaatccc cgtagttggc ccgctgccct 26580 ggtgtaccag gaaagtcccg ctcccaccac tgtggtactt cccagagacg cccaggccga 26640 agttcagatg actaactcag gggcgcagct tgcgggcggc tttcgtcaca gggtgcggtc 26700 gcccgggcag ggtataactc acctgacaat cagagggcga ggtattcagc tcaacgacga 26760 gtcggtgagc tcctcgcttg gtctccgtcc ggacgggaca tttcagatcg gcggcgccgg 26820 ccgtccttca ttcacgcctc gtcaggcaat cctaactctg cagacctcgt cctctgagcc 26880 gcgctctgga ggcattggaa ctctgcaatt tattgaggag tttgtgccat cggtctactt 26940 taaccccttc tcgggacctc ccggccacta tccggatcaa tttattccta actttgacgc 27000 ggtaaaggac tcggcggacg gctacgactg aatgttaatt aagttcctgt ccatccgcac 27060 ccactatctt catgttgttg cagatgaagc gcgcaagacc gtctgaagat accttcaacc 27120 ccgtgtatcc atatgacacg gaaaccggtc ctccaactgt gccttttctt actcctccct 27180 ttgtatcccc caatgggttt caagagagtc cccctggggt actctctttg cgcctatccg 27240 aacctctagt tacctccaat ggcatgcttg cgctcaaaat gggcaacggc ctctctctgg 27300 acgaggccgg caaccttacc tcccaaaatg taaccactgt gagcccacct ctcaaaaaaa 27360 ccaagtcaaa cataaacctg gaaatatctg cacccctcac agttacctca gaagccctaa 27420 ctgtggctgc cgccgcacct ctaatggtcg cgggcaacac actcaccatg caatcacagg 27480 ccccgctaac cgtgcacgac tccaaactta gcattgccac ccaaggaccc ctcacagtgt 27540 cagaaggaaa gctagccctg caaacatcag gccccctcac caccaccgat agcagtaccc 27600 ttactatcac tgcctcaccc cctctaacta ctgccactgg tagcttgggc attgacttga 27660 aagagcccat ttatacacaa aatggaaaac taggactaaa gtacggggct cctttgcatg 27720 taacagacga cctaaacact ttgaccgtag caactggtcc aggtgtgact attaataata 27780 cttccttgca aactaaagtt actggagcct tgggttttga ttcacaaggc aatatgcaac 27840 ttaatgtagc aggaggacta aggattgatt ctcaaaacag acgccttata cttgatgtta 27900 gttatccgtt tgatgctcaa aaccaactaa atctaagact aggacagggc cctcttttta 27960 taaactcagc ccacaacttg gatattaact acaacaaagg cctttacttg tttacagctt 28020 caaacaattc caaaaagctt gaggttaacc taagcactgc caaggggttg atgtttgacg 28080 ctacagccat agccattaat gcaggagatg ggcttgaatt tggttcacct aatgcaccaa 28140 acacaaatcc cctcaaaaca aaaattggcc atggcctaga atttgattca aacaaggcta 28200 tggttcctaa actaggaact ggccttagtt ttgacagcac aggtgccatt acagtaggaa 28260 acaaaaataa tgataagcta actttgtgga ccacaccagc tccatctcct aactgtagac 28320 taaatgcaga gaaagatgct aaactcactt tggtcttaac aaaatgtggc agtcaaatac 28380 ttgctacagt ttcagttttg gctgttaaag gcagtttggc tccaatatct ggaacagttc 28440 aaagtgctca tcttattata agatttgacg aaaatggagt gctactaaac aattccttcc 28500 tggacccaga atattggaac tttagaaatg gagatcttac tgaaggcaca gcctatacaa 28560 acgctgttgg atttatgcct aacctatcag cttatccaaa atctcacggt aaaactgcca 28620 aaagtaacat tgtcagtcaa gtttacttaa acggagacaa aactaaacct gtaacactaa 28680 ccattacact aaacggtaca caggaaacag gagacacaac tccaagtgca tactctatgt 28740 cattttcatg ggactggtct ggccacaact acattaatga aatatttgcc acatcctctt 28800 acactttttc atacattgcc caagaataaa gaatcgtttg tgttatgttt caacgtgttt 28860 atttttcaat tgcagaaaat ttcaagtcat ttttcattca gtagtatagc cccaccacca 28920 catagcttat acagatcacc gtaccttaat caaactcaca gaaccctagt attcaacctg 28980 ccacctccct cccaacacac agagtacaca gtcctttctc cccggctggc cttaaaaagc 29040 atcatatcat gggtaacaga catattctta ggtgttatat tccacacggt ttcctgtcga 29100 gccaaacgct catcagtgat attaataaac tccccgggca gctcacttaa gttcatgtcg 29160 ctgtccagct gctgagccac aggctgctgt ccaacttgcg gttgcttaac gggcggcgaa 29220 ggagaagtcc acgcctacat gggggtagag tcataatcgt gcatcaggat agggcggtgg 29280 tgctgcagca gcgcgcgaat aaactgctgc cgccgccgct ccgtcctgca ggaatacaac 29340 atggcagtgg tctcctcagc gatgattcgc accgcccgca gcataaggcg ccttgtcctc 29400 cgggcacagc agcgcaccct gatctcactt aaatcagcac agtaactgca gcacagcacc 29460 acaatattgt tcaaaatccc acagtgcaag gcgctgtatc caaagctcat ggcggggacc 29520 acagaaccca cgtggccatc ataccacaag cgcaggtaga ttaagtggcg acccctcata 29580 aacacgctgg acataaacat tacctctttt ggcatgttgt aattcaccac ctcccggtac 29640 catataaacc tctgattaaa catggcgcca tccaccacca tcctaaacca gctggccaaa 29700 acctgcccgc cggctataca ctgcagggaa ccgggactgg aacaatgaca gtggagagcc 29760 caggactcgt aaccatggat catcatgctc gtcatgatat caatgttggc acaacacagg 29820 cacacgtgca tacacttcct caggattaca agctcctccc gcgttagaac catatcccag 29880 ggaacaaccc attcctgaat cagcgtaaat cccacactgc agggaagacc tcgcacgtaa 29940 ctcacgttgt gcattgtcaa agtgttacat tcgggcagca gcggatgatc ctccagtatg 30000 gtagcgcggg tttctgtctc aaaaggaggt agacgatccc tactgtacgg agtgcgccga 30060 gacaaccgag atcgtgttgg tcgtagtgtc atgccaaatg gaacgccgga cgtagtcata 30120 tttcctgaag caaaaccagg tgcgggcgtg acaaacagat ctgcgtctcc ggtctcgccg 30180 cttagatcgc tctgtgtagt agttgtagta tatccactct ctcaaagcat ccaggcgccc 30240 cctggcttcg ggttctatgt aaactccttc atgcgccgct gccctgataa catccaccac 30300 cgcagaataa gccacaccca gccaacctac acattcgttc tgcgagtcac acacgggagg 30360 agcgggaaga gctggaagaa ccatgttttt ttttttattc caaaagatta tccaaaacct 30420 caaaatgaag atctattaag tgaacgcgct cccctccggt ggcgtggtca aactctacag 30480 ccaaagaaca gataatggca tttgtaagat gttgcacaat ggcttccaaa aggcaaacgg 30540 ccctcacgtc caagtggacg taaaggctaa acccttcagg gtgaatctcc tctataaaca 30600 ttccagcacc ttcaaccatg cccaaataat tctcatctcg ccaccttctc aatatatctc 30660 taagcaaatc ccgaatatta agtccggcca ttgtaaaaat ctgctccaga gcgccctcca 30720 ccttcagcct caagcagcga atcatgattg caaaaattca ggttcctcac agacctgtat 30780 aagattcaaa agcggaacat taacaaaaat accgcgatcc cgtaggtccc ttcgcagggc 30840 cagctgaaca taatcgtgca ggtctgcacg gaccagcgcg gccacttccc cgccaggaac 30900 cttgacaaaa gaacccacac tgattatgac acgcatactc ggagctatgc taaccagcgt 30960 agccccgatg taagctttgt tgcatgggcg gcgatataaa atgcaaggtg ctgctcaaaa 31020 aatcaggcaa agcctcgcgc aaaaaagaaa gcacatcgta gtcatgctca tgcagataaa 31080 ggcaggtaag ctccggaacc accacagaaa aagacaccat ttttctctca aacatgtctg 31140 cgggtttctg cataaacaca aaataaaata acaaaaaaac atttaaacat tagaagcctg 31200 tcttacaaca ggaaaaacaa cccttataag cataagacgg actacggcca tgccggcgtg 31260 accgtaaaaa aactggtcac cgtgattaaa aagcaccacc gacagctcct cggtcatgtc 31320 cggagtcata atgtaagact cggtaaacac atcaggttga ttcatcggtc agtgctaaaa 31380 agcgaccgaa atagcccggg ggaatacata cccgcaggcg tagagacaac attacagccc 31440 ccataggagg tataacaaaa ttaataggag agaaaaacac ataaacacct gaaaaaccct 31500 cctgcctagg caaaatagca ccctcccgct ccagaacaac atacagcgct tcacagcggc 31560 agcctaacag tcagccttac cagtaaaaaa gaaaacctat taaaaaaaca ccactcgaca 31620 cggcaccagc tcaatcagtc acagtgtaaa aaagggccaa gtgcagagcg agtatatata 31680 ggactaaaaa atgacgtaac ggttaaagtc cacaaaaaac acccagaaaa ccgcacgcga 31740 acctacgccc agaaacgaaa gccaaaaaac ccacaacttc ctcaaatcgt cacttccgtt 31800 ttcccacgtt acgtaacttc ccattttaag aaaactacaa ttcccaacac atacaagtta 31860 ctccgcccta aaacctacgt cacccgcccc gttcccacgc cccgcgccac gtcacaaact 31920 ccaccccctc attatcatat tggcttcaat ccaaaataag gtatattatt gatgat 31976 2 31976 DNA adenovirus 2 catcatcaat aatatacctt attttggatt gaagccaata tgataatgag ggggtggagt 60 ttgtgacgtg gcgcggggcg tgggaacggg gcgggtgacg tagtagtgtg gcggaagtgt 120 gatgttgcaa gtgtggcgga acacatgtaa gcgacggatg tggcaaaagt gacgtttttg 180 gtgtgcgccg gtgtacacag gaagtgacaa ttttcgcgcg gttttaggcg gatgttgtag 240 taaatttggg cgtaaccgag taagatttgg ccattttcgc gggaaaactg aataagagga 300 agtgaaatct gaataatttt gtgttactca tagcgcgtaa tatttgtcta gggccgcggg 360 gactttgacc gtttacgtgg agactcgccc aggtgttttt ctcaggtgtt ttccgcgttc 420 cgggtcaaag ttggcgtttt attattatag tcagctgacg tgtagtgtat ttatacccgg 480 tgagttcctc aagaggccac tcttgagtgc cagcgagtag agttttctcc tccgagccgc 540 tccgacaccg ggactgaaaa tgagacatat tatctgccac ggaggtgtta ttaccgaaga 600 aatggccgcc agtcttttgg accagctgat cgaagaggta ctggctgata atcttccacc 660 tcctagccat tttgaaccac ctacccttca cgaactgtat gatttagacg tgacggcccc 720 cgaagatccc aacgaggagg cggtttcgca gatttttccc gactctgtaa tgttggcggt 780 gcaggaaggg attgacttac tcacttttcc gccggcgccc ggttctccgg agccgcctca 840 cctttcccgg cagcccgagc agccggagca gagagccttg ggtccggttt ctatgccaaa 900 ccttgtaccg gaggtgatcg atcttacctg ccacgaggct ggctttccac ccagtgacga 960 cgaggatgaa gagggtgagg agtttgtgtt agattatgtg gagcaccccg ggcacggttg 1020 caggtcttgt cattatcacc ggaggaatac gggggaccca gatattatgt gttcgctttg 1080 ctatatgagg acctgtggca tgtttgtcta cagtaagtga aaattatggg cagtgggtga 1140 tagagtggtg ggtttggtgt ggtaattttt tttttaattt ttacagtttt gtggtttaaa 1200 gaattttgta ttgtgatttt tttaaaaggt cctgtgtctg aacctgagcc tgagcccgag 1260 ccagaaccgg agcctgcaag acctacccgc cgtcctaaaa tggcgcctgc tatcctgaga 1320 cgcccgacat cacctgtgtc tagagaatgc aatagtagta cggatagctg tgactccggt 1380 ccttctaaca cacctcctga gatacacccg gtggtcccgc tgtgccccat taaaccagtt 1440 gccgtgagag ttggtgggcg tcgccaggct gtggaatgta tcgaggactt gcttaacgag 1500 cctgggcaac ctttggactt gagctgtaaa cgccccaggc cataaggtgt aaacctgtga 1560 ttgcgtgtgt ggttaacgcc tttgtttgct gaatgagttg atgtaagttt aataaagggt 1620 gagataatgt ttaacttgca tggcgtgtta aatggggcgg ggcttaaagg gtatataatg 1680 cgccgtgggc taatcttggt tacatctgac ctcatggagg cttgggagtg tttggaagat 1740 ttttctgctg tgcgtaactt gctggaacag agctctaaca gtacctcttg gttttggagg 1800 tttctgtggg gctcatccca ggcaaagtta gtctgcagaa ttaaggagga ttacaagtgg 1860 gaatttgaag agcttttgaa atcctgtggt gagctgtttg attctttgaa tctgggtcac 1920 caggcgcttt tccaagagaa ggtcatcaag actttggatt tttccacacc ggggcgcgct 1980 gcggctgctg ttgctttttt gagttttata aaggataaat ggagcgaaga aacccatctg 2040 agcggggggt acctgctgga ttttctggcc atgcatctgt ggagagcggt tgtgagacac 2100 aagaatcgcc tgctactgtt gtcttccgtc cgcccggcga taataccgac ggaggagcag 2160 cagcagcagc aggaggaagc caggcggcgg cggcaggagc agagcccatg gaacccgaga 2220 gccggcctgg accctcggga atgaatgttg tacaggtggc tgaactgtat ccagaactga 2280 gacgcatttt gacaattaca gaggatgggc aggggctaaa gggggtaaag agggagcggg 2340 gggcttgtga ggctacagag gaggctagga atctagcttt tagcttaatg accagacacc 2400 gtcctgagtg tattactttt caacagatca aggataattg cgctaatgag cttgatctgc 2460 tggcgcagaa gtattccata gagcagctga ccacttactg gagatctgga aggtgctgag 2520 gtacgatgag acccgcacca ggtgcagacc ctgcgagtgt ggcggtaaac atattaggaa 2580 ccagcctgtg atgctggatg tgaccgagga gctgaggccc gatcacttgg tgctggcctg 2640 cacccgcgct gagtttggct ctagcgatga agatacagat tgaggtactg aaatgtgtgg 2700 gcgtggctta agggtgggaa agaatatata aggtgggggt cttatgtagt tttgtatctg 2760 ttttgcagca gccgccgccg ccatgagcac caactcgttt gatggaagca ttgtgagctc 2820 atatttgaca acgcgcatgc ccccatgggc cggggtgcgt cagaatgtga tgggctccag 2880 cattgatggt cgccccgtcc tgcccgcaaa ctctactacc ttgacctacg agaccgtgtc 2940 tggaacgccg ttggagactg cagcctccgc cgccgcttca gccgctgcag ccaccgcccg 3000 cgggattgtg actgactttg ctttcctgag cccgcttgca agcagtgcag cttcccgttc 3060 atccgcccgc gatgacaagt tgacggctct tttggcacaa ttggattctt tgacccggga 3120 acttaatgtc gtttctcagc agctgttgga tctgcgccag caggtttctg ccctgaaggc 3180 ttcctcccct cccaatgcgg tttaaaacat aaataaaaaa ccagactctg tttggatttg 3240 gatcaagcaa gtgtcttgct gtctttattt aggggttttg cgcgcgcggt aggcccggga 3300 ccagcggtct cggtcgttga gggtcctgtg tattttttcc aggacgtggt aaaggtgact 3360 ctggatgttc agatacatgg gcataagccc gtctctgggg tggaggtagc accactgcag 3420 agcttcatgc tgcggggtgg tgttgtagat gatccagtcg tagcaggagc gctgggcgtg 3480 gtgcctaaaa atgtctttca gtagcaagct gattgccagg ggcaggccct tggtgtaagt 3540 gtttacaaag cggttaagct gggatgggtg catacgtggg gatatgagat gcatcttgga 3600 ctgtattttt aggttggcta tgttcccagc catatccctc cggggattca tgttgtgcag 3660 aaccaccagc acagtgtatc cggtgcactt gggaaatttg tcatgtagct tagaaggaaa 3720 tgcgtggaag aacttggaga cgcccttgtg acctccaaga ttttccatgc attcgtccat 3780 aatgatggca atgggcccac gggcggcggc ctgggcgaag atatttctgg gatcactaac 3840 gtcatagttg tgttccagga tgagatcgtc ataggccatt tttacaaagc gcgggcggag 3900 ggtgccagac tgcggtataa tggttccatc cggcccaggg gcgtagttac cctcacagat 3960 ttgcatttcc cacgctttga gttcagatgg ggggatcatg tctacctgcg gggcgatgaa 4020 gaaaacggtt tccggggtag gggagatcag ctgggaagaa agcaggttcc tgagcagctg 4080 cgacttaccg cagccggtgg gcccgtaaat cacacctatt accgggtgca actggtagtt 4140 aagagagctg cagctgccgt catccctgag caggggggcc acttcgttaa gcatgtccct 4200 gactcgcatg ttttccctga ccaaatccgc cagaaggcgc tcgccgccca gcgatagcag 4260 ttcttgcaag gaagcaaagt ttttcaacgg tttgagaccg tccgccgtag gcatgctttt 4320 gagcgtttga ccaagcagtt ccaggcggtc ccacagctcg gtcacctgct ctacggcatc 4380 tcgatccagc atatctcctc gtttcgcggg ttggggcggc tttcgctgta cggcagtagt 4440 cggtgctcgt ccagacgggc cagggtcatg tctttccacg ggcgcagggt cctcgtcagc 4500 gtagtctggg tcacggtgaa ggggtgcgct ccgggctgcg cgctggccag ggtgcgcttg 4560 aggctggtcc tgctggtgct gaagcgctgc cggtcttcgc cctgcgcgtc ggccaggtag 4620 catttgacca tggtgtcata gtccagcccc tccgcggcgt ggcccttggc gcgcagcttg 4680 cccttggagg aggcgccgca cgaggggcag tgcagacttt tgagggcgta gagcttgggc 4740 gcgagaaata ccgattccgg ggagtaggca tccgcgccgc aggccccgca gacggtctcg 4800 cattccacga gccaggtgag ctctggccgt tcggggtcaa aaaccaggtt tcccccatgc 4860 tttttgatgc gtttcttacc tctggtttcc atgagccggt gtccacgctc ggtgacgaaa 4920 aggctgtccg tgtccccgta tacagacttg agaggcctgt cctcgagcgg tgttccgcgg 4980 tcctcctcgt atagaaactc ggaccactct gagacaaagg ctcgcgtcca ggccagcacg 5040 aaggaggcta agtgggaggg gtagcggtcg ttgtccacta gggggtccac tcgctccagg 5100 gtgtgaagac acatgtcgcc ctcttcggca tcaaggaagg tgattggttt gtaggtgtag 5160 gccacgtgac cgggtgttcc tgaagggggg ctataaaagg gggtgggggc gcgttcgtcc 5220 tcactctctt ccgcatcgct gtctgcgagg gccagctgtt ggggtgagta ctccctctga 5280 aaagcgggca tgacttctgc gctaagattg tcagtttcca aaaacgagga ggatttgata 5340 ttcacctggc ccgcggtgat gcctttgagg gtggccgcat ccatctggtc agaaaagaca 5400 atctttttgt tgtcaagctt ggtggcaaac gacccgtaga gggcgttgga cagcaacttg 5460 gcgatggagc gcagggtttg gtttttgtcg cgatcggcgc gctccttggc cgcgatgttt 5520 agctgcacgt attcgcgcgc aacgcaccgc cattcgggaa agacggtggt gcgctcgtcg 5580 ggcaccaggt gcacgcgcca accgcggttg tgcagggtga caaggtcaac gctggtggct 5640 acctctccgc gtaggcgctc gttggtccag cagaggcggc cgcccttgcg cgagcagaat 5700 ggcggtaggg ggtctagctg cgtctcgtcc ggggggtctg cgtccacggt aaagaccccg 5760 ggcagcaggc gcgcgtcgaa gtagtctatc ttgcatcctt gcaagtctag cgcctgctgc 5820 catgcgcggg cggcaagcgc gcgctcgtat gggttgagtg ggggacccca tggcatgggg 5880 tgggtgagcg cggaggcgta catgccgcaa atgtcgtaaa cgtagagggg ctctctgagt 5940 attccaagat atgtagggta gcatcttcca ccgcggatgc tggcgcgcac gtaatcgtat 6000 agttcgtgcg agggagcgag gaggtcggga ccgaggttgc tacgggcggg ctgctctgct 6060 cggaagacta tctgcctgaa gatggcatgt gagttggatg atatggttgg acgctggaag 6120 acgttgaagc tggcgtctgt gagacctacc gcgtcacgca cgaaggaggc gtaggagtcg 6180 cgcagcttgt tgaccagctc ggcggtgacc tgcacgtcta gggcgcagta gtccagggtt 6240 tccttgatga tgtcatactt atcctgtccc ttttttttcc acagctcgcg gttgaggaca 6300 aactcttcgc ggtctttcca gtactcttgg atcggaaacc cgtcggcctc cgaacggtaa 6360 gagcctagca tgtagaactg gttgacggcc tggtaggcgc agcatccctt ttctacgggt 6420 agcgcgtatg cctgcgcggc cttccggagc gaggtgtggg tgagcgcaaa ggtgtccctg 6480 accatgactt tgaggtactg gtatttgaag tcagtgtcgt cgcatccgcc ctgctcccag 6540 agcaaaaagt ccgtgcgctt tttggaacgc ggatttggca gggcgaaggt gacatcgttg 6600 aagagtatct ttcccgcgcg aggcataaag ttgcgtgtga tgcggaaggg tcccggcacc 6660 tcggaacggt tgttaattac ctgggcggcg agcacgatct cgtcaaagcc gttgatgttg 6720 tggcccacaa tgtaaagttc caagaagcgc gggatgccct tgatggaagg caatttttta 6780 agttcctcgt aggtgagctc ttcaggggag ctgagcccgt gctctgaaag ggcccagtct 6840 gcaagatgag ggttggaagc gacgaatgag ctccacaggt cacgggccat tagcatttgc 6900 aggtggtcgc gaaaggtcct aaactggcga cctatggcca ttttttctgg ggtgatgcag 6960 tagaaggtaa gcgggtcttg ttcccagcgg tcccatccaa ggttcgcggc taggtctcgc 7020 gcggcagtca ctagaggctc atctccgccg aacttcatga ccagcatgaa gggcacgagc 7080 tgcttcccaa aggcccccat ccaagtatag gtctctacat cgtaggtgac aaagagacgc 7140 tcggtgcgag gatgcgagcc gatcgggaag aactggatct cccgccacca attggaggag 7200 tggctattga tgtggtgaaa gtagaagtcc ctgcgacggg ccgaacactc gtgctggctt 7260 ttgtaaaaac gtgcgcagta ctggcagcgg tgcacgggct gtacatcctg cacgaggttg 7320 acctgacgac cgcgcacaag gaagcagagt gggaatttga gcccctcgcc tggcgggttt 7380 ggctggtggt cttctacttc ggctgcttgt ccttgaccgt ctggctgctc gaggggagtt 7440 acggtggatc ggaccaccac gccgcgcgag cccaaagtcc agatgtccgc gcgcggcggt 7500 cggagcttga tgacaacatc gcgcagatgg gagctgtcca tggtctggag ctcccgcggc 7560 gtcaggtcag gcgggagctc ctgcaggttt acctcgcata gacgggtcag ggcgcgggct 7620 agatccaggt gatacctaat ttccaggggc tggttggtgg cggcgtcgat ggcttgcaag 7680 aggccgcatc cccgcggcgc gactacggta ccgcgcggcg ggcggtgggc cgcgggggtg 7740 tccttggatg atgcatctaa aagcggtgac gcgggcgagc ccccggaggt agggggggct 7800 ccggacccgc cgggagaggg ggcaggggca cgtcggcgcc gcgcgcgggc aggagctggt 7860 gctgcgcgcg taggttgctg gcgaacgcga cgacgcggcg gttgatctcc tgaatctggc 7920 gcctctgcgt gaagacgacg ggcccggtga gcttgagcct gaaagagagt tcgacagaat 7980 caatttcggt gtcgttgacg gcggcctggc gcaaaatctc ctgcacgtct cctgagttgt 8040 cttgataggc gatctcggcc atgaactgct cgatctcttc ctcctggaga tctccgcgtc 8100 cggctcgctc cacggtggcg gcgaggtcgt tggaaatgcg ggccatgagc tgcgagaagg 8160 cgttgaggcc tccctcgttc cagacgcggc tgtagaccac gcccccttcg gcatcgcggg 8220 cgcgcatgac cacctgcgcg agattgagct ccacgtgccg ggcgaagacg gcgtagtttc 8280 gcaggcgctg aaagaggtag ttgagggtgg tggcggtgtg ttctgccacg aagaagtaca 8340 taacccagcg tcgcaacgtg gattcgttga tatcccccaa ggcctcaagg cgctccatgg 8400 cctcgtagaa gtccacggcg aagttgaaaa actgggagtt gcgcgccgac acggttaact 8460 cctcctccag aagacggatg agctcggcga cagtgtcgcg cacctcgcgc tcaaaggcta 8520 caggggcctc ttcttcttct tcaatctcct cttccataag ggcctcccct tcttcttctt 8580 ctggcggcgg tgggggaggg gggacacggc ggcgacgacg gcgcaccggg aggcggtcga 8640 caaagcgctc gatcatctcc ccgcggcgac ggcgcatggt ctcggtgacg gcgcggccgt 8700 tctcgcgggg gcgcagttgg aagacgccgc ccgtcatgtc ccggttatgg gttggcgggg 8760 ggctgccatg cggcagggat acggcgctaa cgatgcatct caacaattgt tgtgtaggta 8820 ctccgccgcc gagggacctg agcgagtccg catcgaccgg atcggaaaac ctctcgagaa 8880 aggcgtctaa ccagtcacag tcgcaaggta ggctgagcac cgtggcgggc ggcagcgggc 8940 ggcggtcggg gttgtttctg gcggaggtgc tgctgatgat gtaattaaag taggcggtct 9000 tgagacggcg gatggtcgac agaagcacca tgtccttggg tccggcctgc tgaatgcgca 9060 ggcggtcggc catgccccag gcttcgtttt gacatcggcg caggtctttg tagtagtctt 9120 gcatgagcct ttctaccggc acttcttctt ctccttcctc ttgtcctgca tctcttgcat 9180 ctatcgctgc ggcggcggcg gagtttggcc gtaggtggcg ccctcttcct cccatgcgtg 9240 tgaccccgaa gcccctcatc ggctgaagca gggctaggtc ggcgacaacg cgctcggcta 9300 atatggcctg ctgcacctgc gtgagggtag actggaagtc atccatgtcc acaaagcggt 9360 ggtatgcgcc cgtgttgatg gtgtaagtgc agttggccat aacggaccag ttaacggtct 9420 ggtgacccgg ctgcgagagc tcggtgtacc tgagacgcga gtaagccctc gagtcaaata 9480 cgtagtcgtt gcaagtccgc accaggtact ggtatcccac caaaaagtgc ggcggcggct 9540 ggcggtagag gggccagcgt agggtggccg gggctccggg ggcgagatct tccaacataa 9600 ggcgatgata tccgtagatg tacctggaca tccaggtgat gccggcggcg gtggtggagg 9660 cgcgcggaaa gtcgcggacg cggttccaga tgttgcgcag cggcaaaaag tgctccatgg 9720 tcgggacgct ctggccggtc aggcgcgcgc aatcgttgac gctctagacc gtgcaaaagg 9780 agagcctgta agcgggcact cttccgtggt ctggtggata aattcgcaag ggtatcatgg 9840 cggacgaccg gggttcgagc cccgtatccg gccgtccgcc gtgatccatg cggttaccgc 9900 ccgcgtgtcg aacccaggtg tgcgacgtca gacaacgggg gagtgctcct tttggcttcc 9960 ttccaggcgc ggcggctgct gcgctagctt ttttggccac tggccgcgcg cagcgtaagc 10020 ggttaggctg gaaagcgaaa gcattaagtg gctcgctccc tgtagccgga gggttatttt 10080 ccaagggttg agtcgcggga cccccggttc gagtctcgga ccggccggac tgcggcgaac 10140 gggggtttgc ctccccgtca tgcaagaccc cgcttgcaaa ttcctccgga aacagggacg 10200 agcccctttt ttgcttttcc cagatgcatc cggtgctgcg gcagatgcgc ccccctcctc 10260 agcagcggca agagcaagag cagcggcaga catgcagggc accctcccct cctcctaccg 10320 cgtcaggagg ggcgacatcc gcggttgacg cggcagcaga tggtgattac gaacccccgc 10380 ggcgccgggc ccggcactac ctggacttgg aggagggcga gggcctggcg cggctaggag 10440 cgccctctcc tgagcggtac ccaagggtgc agctgaagcg tgatacgcgt gaggcgtacg 10500 tgccgcggca gaacctgttt cgcgaccgcg agggagagga gcccgaggag atgcgggatc 10560 gaaagttcca cgcagggcgc gagctgcggc atggcctgaa tcgcgagcgg ttgctgcgcg 10620 aggaggactt tgagcccgac gcgcgaaccg ggattagtcc cgcgcgcgca cacgtggcgg 10680 ccgccgacct ggtaaccgca tacgagcaga cggtgaacca ggagattaac tttcaaaaaa 10740 gctttaacaa ccacgtgcgt acgcttgtgg cgcgcgagga ggtggctata ggactgatgc 10800 atctgtggga ctttgtaagc gcgctggagc aaaacccaaa tagcaagccg ctcatggcgc 10860 agctgttcct tatagtgcag cacagcaggg acaacgaggc attcagggat gcgctgctaa 10920 acatagtaga gcccgagggc cgctggctgc tcgatttgat aaacatcctg cagagcatag 10980 tggtgcagga gcgcagcttg agcctggctg acaaggtggc cgccatcaac tattccatgc 11040 ttagcctggg caagttttac gcccgcaaga tataccatac cccttacgtt cccatagaca 11100 aggaggtaaa gatcgagggg ttctacatgc gcatggcgct gaaggtgctt accttgagcg 11160 acgacctggg cgtttatcgc aacgagcgca tccacaaggc cgtgagcgtg agccggcggc 11220 gcgagctcag cgaccgcgag ctgatgcaca gcctgcaaag ggccctggct ggcacgggca 11280 gcggcgatag agaggccgag tcctactttg acgcgggcgc tgacctgcgc tgggccccaa 11340 gccgacgcgc cctggaggca gctggggccg gacctgggct ggcggtggca cccgcgcgcg 11400 ctggcaacgt cggcggcgtg gaggaatatg acgaggacga tgagtacgag ccagaggacg 11460 gcgagtacta agcggtgatg tttctgatca gatgatgcaa gacgcaacgg acccggcggt 11520 gcgggcggcg ctgcagagcc agccgtccgg ccttaactcc acggacgact ggcgccaggt 11580 catggaccgc atcatgtcgc tgactgcgcg caatcctgac gcgttccggc agcagccgca 11640 ggccaaccgg ctctccgcaa ttctggaagc ggtggtcccg gcgcgcgcaa accccacgca 11700 cgagaaggtg ctggcgatcg taaacgcgct ggccgaaaac agggccatcc ggcccgacga 11760 ggccggcctg gtctacgacg cgctgcttca gcgcgtggct cgttacaaca gcggcaacgt 11820 gcagaccaac ctggaccggc tggtggggga tgtgcgcgag gccgtggcgc agcgtgagcg 11880 cgcgcagcag cagggcaacc tgggctccat ggttgcacta aacgccttcc tgagtacaca 11940 gcccgccaac gtgccgcggg gacaggagga ctacaccaac tttgtgagcg cactgcggct 12000 aatggtgact gagacaccgc aaagtgaggt gtaccagtct gggccagact attttttcca 12060 gaccagtaga caaggcctgc agaccgtaaa cctgagccag gctttcaaaa acttgcaggg 12120 gctgtggggg gtgcgggctc ccacaggcga ccgcgcgacc gtgtctagct tgctgacgcc 12180 caactcgcgc ctgttgctgc tgctaatagc gcccttcacg gacagtggca gcgtgtcccg 12240 ggacacatac ctaggtcact tgctgacact gtaccgcgag gccataggtc aggcgcatgt 12300 ggacgagcat actttccagg agattacaag tgtcagccgc gcgctggggc aggaggacac 12360 gggcagcctg gaggcaaccc taaactacct gctgaccaac cggcggcaga agatcccctc 12420 gttgcacagt ttaaacagcg aggaggagcg cattttgcgc tacgtgcagc agagcgtgag 12480 ccttaacctg atgcgcgacg gggtaacgcc cagcgtggcg ctggacatga ccgcgcgcaa 12540 catggaaccg ggcatgtatg cctcaaaccg gccgtttatc aaccgcctaa tggactactt 12600 gcatcgcgcg gccgccgtga accccgagta tttcaccaat gccatcttga acccgcactg 12660 gctaccgccc cctggtttct acaccggggg attcgaggtg cccgagggta acgatggatt 12720 cctctgggac gacatagacg acagcgtgtt ttccccgcaa ccgcagaccc tgctagagtt 12780 gcaacagcgc gagcaggcag aggcggcgct gcgaaaggaa agcttccgca ggccaagcag 12840 cttgtccgat ctaggcgctg cggccccgcg gtcagatgct agtagcccat ttccaagctt 12900 gatagggtct cttaccagca ctcgcaccac ccgcccgcgc ctgctgggcg aggaggagta 12960 cctaaacaac tcgctgctgc agccgcagcg cgaaaaaaac ctgcctccgg catttcccaa 13020 caacgggata gagagcctag tggacaagat gagtagatgg aagacgtacg cgcaggagca 13080 cagggacgtg ccaggcccgc gcccgcccac ccgtcgtcaa aggcacgacc gtcagcgggg 13140 tctggtgtgg gaggacgatg actcggcaga cgacagcagc gtcctggatt tgggagggag 13200 tggcaacccg tttgcgcacc ttcgccccag gctggggaga atgttttaaa aaaaaaaaag 13260 catgatgcaa aataaaaaac tcaccaaggc catggcaccg agcgttggtt ttcttgtatt 13320 ccccttagta tgcggcgcgc ggcgatgtat gaggaaggtc ctcctccctc ctacgagagt 13380 gtggtgagcg cggcgccagt ggcggcggcg ctgggttctc ccttcgatgc tcccctggac 13440 ccgccgtttg tgcctccgcg gtacctgcgg cctaccgggg ggagaaacag catccgttac 13500 tctgagttgg cacccctatt cgacaccacc cgtgtgtacc tggtggacaa caagtcaacg 13560 gatgtggcat ccctgaacta ccagaacgac cacagcaact ttctgaccac ggtcattcaa 13620 aacaatgact acagcccggg ggaggcaagc acacagacca tcaatcttga cgaccggtcg 13680 cactggggcg gcgacctgaa aaccatcctg cataccaaca tgccaaatgt gaacgagttc 13740 atgtttacca ataagtttaa ggcgcgggtg atggtgtcgc gcttgcctac taaggacaat 13800 caggtggagc tgaaatacga gtgggtggag ttcacgctgc ccgagggcaa ctactccgag 13860 accatgacca tagaccttat gaacaacgcg atcgtggagc actacttgaa agtgggcaga 13920 cagaacgggg ttctggaaag cgacatcggg gtaaagtttg acacccgcaa cttcagactg 13980 gggtttgacc ccgtcactgg tcttgtcatg cctggggtat atacaaacga agccttccat 14040 ccagacatca ttttgctgcc aggatgcggg gtggacttca cccacagccg cctgagcaac 14100 ttgttgggca tccgcaagcg gcaacccttc caggagggct ttaggatcac ctacgatgat 14160 ctggagggtg gtaacattcc cgcactgttg gatgtggacg cctaccaggc gagcttgaaa 14220 gatgacaccg aacagggcgg gggtggcgca ggcggcagca acagcagtgg cagcggcgcg 14280 gaagagaact ccaacgcggc agccgcggca atgcagccgg tggaggacat gaacgatcat 14340 gccattcgcg gcgacacctt tgccacacgg gctgaggaga agcgcgctga ggccgaagca 14400 gcggccgaag ctgccgcccc cgctgcgcaa cccgaggtcg agaagcctca gaagaaaccg 14460 gtgatcaaac ccctgacaga ggacagcaag aaacgcagtt acaacctaat aagcaatgac 14520 agcaccttca cccagtaccg cagctggtac cttgcataca actacggcga ccctcagacc 14580 ggaatccgct catggaccct gctttgcact cctgacgtaa cctgcggctc ggagcaggtc 14640 tactggtcgt tgccagacat gatgcaagac cccgtgacct tccgctccac gcgccagatc 14700 agcaactttc cggtggtggg cgccgagctg ttgcccgtgc actccaagag cttctacaac 14760 gaccaggccg tctactccca actcatccgc cagtttacct ctctgaccca cgtgttcaat 14820 cgctttcccg agaaccagat tttggcgcgc ccgccagccc ccaccatcac caccgtcagt 14880 gaaaacgttc ctgctctcac agatcacggg acgctaccgc tgcgcaacag catcggagga 14940 gtccagcgag tgaccattac tgacgccaga cgccgcacct gcccctacgt ttacaaggcc 15000 ctgggcatag tctcgccgcg cgtcctatcg agccgcactt tttgagcaag catgtccatc 15060 cttatatcgc ccagcaataa cacaggctgg ggcctgcgct tcccaagcaa gatgtttggc 15120 ggggccaaga agcgctccga ccaacaccca gtgcgcgtgc gcgggcacta ccgcgcgccc 15180 tggggcgcgc acaaacgcgg ccgcactggg cgcaccaccg tcgatgacgc catcgacgcg 15240 gtggtggagg aggcgcgcaa ctacacgccc acgccgccac cagtgtccac agtggacgcg 15300 gccattcaga ccgtggtgcg cggagcccgg cgctatgcta aaatgaagag acggcggagg 15360 cgcgtagcac gtcgccaccg ccgccgaccc ggcactgccg cccaacgcgc ggcggcggcc 15420 ctgcttaacc gcgcacgtcg caccggccga cgggcggcca tgcgggccgc tcgaaggctg 15480 gccgcgggta ttgtcactgt gccccccagg tccaggcgac gagcggccgc cgcagcagcc 15540 gcggccatta gtgctatgac tcagggtcgc aggggcaacg tgtattgggt gcgcgactcg 15600 gttagcggcc tgcgcgtgcc cgtgcgcacc cgccccccgc gcaactagat tgcaagaaaa 15660 aactacttag actcgtactg ttgtatgtat ccagcggcgg cggcgcgcaa cgaagctatg 15720 tccaagcgca aaatcaaaga agagatgctc caggtcatcg cgccggagat ctatggcccc 15780 ccgaagaagg aagagcagga ttacaagccc cgaaagctaa agcgggtcaa aaagaaaaag 15840 aaagatgatg atgatgaact tgacgacgag gtggaactgc tgcacgctac cgcgcccagg 15900 cgacgggtac agtggaaagg tcgacgcgta aaacgtgttt tgcgacccgg caccaccgta 15960 gtctttacgc ccggtgagcg ctccacccgc acctacaagc gcgtgtatga tgaggtgtac 16020 ggcgacgagg acctgcttga gcaggccaac gagcgcctcg gggagtttgc ctacggaaag 16080 cggcataagg acatgctggc gttgccgctg gacgagggca acccaacacc tagcctaaag 16140 cccgtaacac tgcagcaggt gctgcccgcg cttgcaccgt ccgaagaaaa gcgcggccta 16200 aagcgcgagt ctggtgactt ggcacccacc gtgcagctga tggtacccaa gcgccagcga 16260 ctggaagatg tcttggaaaa aatgaccgtg gaacctgggc tggagcccga ggtccgcgtg 16320 cggccaatca agcaggtggc gccgggactg ggcgtgcaga ccgtggacgt tcagataccc 16380 actaccagta gcaccagtat tgccaccgcc acagagggca tggagacaca aacgtccccg 16440 gttgcctcag cggtggcgga tgccgcggtg caggcggtcg ctgcggccgc gtccaagacc 16500 tctacggagg tgcaaacgga cccgtggatg tttcgcgttt cagccccccg gcgcccgcgc 16560 ggttcgagga agtacggcgc cgccagcgcg ctactgcccg aatatgccct acatccttcc 16620 attgcgccta cccccggcta tcgtggctac acctaccgcc ccagaagacg agcaactacc 16680 cgacgccgaa ccaccactgg aacccgccgc cgccgtcgcc gtcgccagcc cgtgctggcc 16740 ccgatttccg tgcgcagggt ggctcgcgaa ggaggcagga ccctggtgct gccaacagcg 16800 cgctaccacc ccagcatcgt ttaaaagccg gtctttgtgg ttcttgcaga tatggccctc 16860 acctgccgcc tccgtttccc ggtgccggga ttccgaggaa gaatgcaccg taggaggggc 16920 atggccggcc acggcctgac gggcggcatg cgtcgtgcgc accaccggcg gcggcgcgcg 16980 tcgcaccgtc gcatgcgcgg cggtatcctg cccctcctta ttccactgat cgccgcggcg 17040 attggcgccg tgcccggaat tgcatccgtg gccttgcagg cgcagagaca ctgattaaaa 17100 acaagttgca tgtggaaaaa tcaaaataaa aagtctggac tctcacgctc gcttggtcct 17160 gtaactattt tgtagaatgg aagacatcaa ctttgcgtct ctggccccgc gacacggctc 17220 gcgcccgttc atgggaaact ggcaagatat cggcaccagc aatatgagcg gtggcgcctt 17280 cagctggggc tcgctgtgga gcggcattaa aaatttcggt tccaccgtta agaactatgg 17340 cagcaaggcc tggaacagca gcacaggcca gatgctgagg gataagttga aagagcaaaa 17400 tttccaacaa aaggtggtag atggcctggc ctctggcatt agcggggtgg tggacctggc 17460 caaccaggca gtgcaaaata agattaacag taagcttgat ccccgccctc ccgtagagga 17520 gcctccaccg gccgtggaga cagtgtctcc agaggggcgt ggcgaaaagc gtccgcgccc 17580 cgacagggaa gaaactctgg tgacgcaaat agacgagcct ccctcgtacg aggaggcact 17640 aaagcaaggc ctgcccacca cccgtcccat cgcgcccatg gctaccggag tgctgggcca 17700 gcacacaccc gtaacgctgg acctgcctcc ccccgccgac acccagcaga aacctgtgct 17760 gccaggcccg accgccgttg ttgtaacccg tcctagccgc gcgtccctgc gccgcgccgc 17820 cagcggtccg cgatcgttgc ggcccgtagc cagtggcaac tggcaaagca cactgaacag 17880 catcgtgggt ctgggggtgc aatccctgaa gcgccgacga tgcttctgaa tagctaacgt 17940 gtcgtatgtg tgtcatgtat gcgtccatgt cgccgccaga ggagctgctg agccgccgcg 18000 cgcccgcttt ccaagatggc taccccttcg atgatgccgc agtggtctta catgcacatc 18060 tcgggccagg acgcctcgga gtacctgagc cccgggctgg tgcagtttgc ccgcgccacc 18120 gagacgtact tcagcctgaa taacaagttt agaaacccca cggtggcgcc tacgcacgac 18180 gtgaccacag accggtccca gcgtttgacg ctgcggttca tccctgtgga ccgtgaggat 18240 actgcgtact cgtacaaggc gcggttcacc ctagctgtgg gtgataaccg tgtgctggac 18300 atggcttcca cgtactttga catccgcggc gtgctggaca ggggccctac ttttaagccc 18360 tactctggca ctgcctacaa cgccctggct cccaagggtg ccccaaatcc ttgcgaatgg 18420 gatgaagctg ctactgctct tgaaataaac ctagaagaag aggacgatga caacgaagac 18480 gaagtagacg agcaagctga gcagcaaaaa actcacgtat ttgggcaggc gccttattct 18540 ggtataaata ttacaaagga gggtattcaa ataggtgtcg aaggtcaaac acctaaatat 18600 gccgataaaa catttcaacc tgaacctcaa ataggagaat ctcagtggta cgaaactgaa 18660 attaatcatg cagctgggag agtccttaaa aagactaccc caatgaaacc atgttacggt 18720 tcatatgcaa aacccacaaa tgaaaatgga gggcaaggca ttcttgtaaa gcaacaaaat 18780 ggaaagctag aaagtcaagt ggaaatgcaa tttttctcaa ctactgaggc gaccgcaggc 18840 aatggtgata acttgactcc taaagtggta ttgtacagtg aagatgtaga tatagaaacc 18900 ccagacactc atatttctta catgcccact attaaggaag gtaactcacg agaactaatg 18960 ggccaacaat ctatgcccaa caggcctaat tacattgctt ttagggacaa ttttattggt 19020 ctaatgtatt acaacagcac gggtaatatg ggtgttctgg cgggccaagc atcgcagttg 19080 aatgctgttg tagatttgca agacagaaac acagagcttt cataccagct tttgcttgat 19140 tccattggtg atagaaccag gtacttttct atgtggaatc aggctgttga cagctatgat 19200 ccagatgtta gaattattga aaatcatgga actgaagatg aacttccaaa ttactgcttt 19260 ccactgggag gtgtgattaa tacagagact cttaccaagg taaaacctaa aacaggtcag 19320 gaaaatggat gggaaaaaga tgctacagaa ttttcagata aaaatgaaat aagagttgga 19380 aataattttg ccatggaaat caatctaaat gccaacctgt ggagaaattt cctgtactcc 19440 aacatagcgc tgtatttgcc cgacaagcta aagtacagtc cttccaacgt aaaaatttct 19500 gataacccaa acacctacga ctacatgaac aagcgagtgg tggctcccgg gttagtggac 19560 tgctacatta accttggagc acgctggtcc cttgactata tggacaacgt caacccattt 19620 aaccaccacc gcaatgctgg cctgcgctac cgctcaatgt tgctgggcaa tggtcgctat 19680 gtgcccttcc acatccaggt gcctcagaag ttctttgcca ttaaaaacct ccttctcctg 19740 ccgggctcat acacctacga gtggaacttc aggaaggatg ttaacatggt tctgcagagc 19800 tccctaggaa atgacctaag ggttgacgga gccagcatta agtttgatag catttgcctt 19860 tacgccacct tcttccccat ggcccacaac accgcctcca cgcttgaggc catgcttaga 19920 aacgacacca acgaccagtc ctttaacgac tatctctccg ccgccaacat gctctaccct 19980 atacccgcca acgctaccaa cgtgcccata tccatcccct cccgcaactg ggcggctttc 20040 cgcggctggg ccttcacgcg ccttaagact aaggaaaccc catcactggg ctcgggctac 20100 gacccttatt acacctactc tggctctata ccctacctag atggaacctt ttacctcaac 20160 cacaccttta agaaggtggc cattaccttt gactcttctg tcagctggcc tggcaatgac 20220 cgcctgctta cccccaacga gtttgaaatt aagcgctcag ttgacgggga gggttacaac 20280 gttgcccagt gtaacatgac caaagactgg ttcctggtac aaatgctagc taactacaac 20340 attggctacc agggcttcta tatcccagag agctacaagg accgcatgta ctccttcttt 20400 agaaacttcc agcccatgag ccgtcaggtg gtggatgata ctaaatacaa ggactaccaa 20460 caggtgggca tcctacacca acacaacaac tctggatttg ttggctacct tgcccccacc 20520 atgcgcgaag gacaggccta ccctgctaac ttcccctatc cgcttatagg caagaccgca 20580 gttgacagca ttacccagaa aaagtttctt tgcgatcgca ccctttggcg catcccattc 20640 tccagtaact ttatgtccat gggcgcactc acagacctgg gccaaaacct tctctacgcc 20700 aactccgccc acgcgctaga catgactttt gaggtggatc ccatggacga gcccaccctt 20760 ctttatgttt tgtttgaagt ctttgacgtg gtccgtgtgc accggccgca ccgcggcgtc 20820 atcgaaaccg tgtacctgcg cacgcccttc tcggccggca acgccacaac ataaagaagc 20880 aagcaacatc aacaacagct gccgccatgg gctccagtga gcaggaactg aaagccattg 20940 tcaaagatct tggttgtggg ccatattttt tgggcaccta tgacaagcgc tttccaggct 21000 ttgtttctcc acacaagctc gcctgcgcca tagtcaatac ggccggtcgc gagactgggg 21060 gcgtacactg gatggccttt gcctggaacc cgcactcaaa aacatgctac ctctttgagc 21120 cctttggctt ttctgaccag cgactcaagc aggtttacca gtttgagtac gagtcactcc 21180 tgcgccgtag cgccattgct tcttcccccg accgctgtat aacgctggaa aagtccaccc 21240 aaagcgtaca ggggcccaac tcggccgcct gtggactatt ctgctgcatg tttctccacg 21300 cctttgccaa ctggccccaa actcccatgg atcacaaccc caccatgaac cttattaccg 21360 gggtacccaa ctccatgctc aacagtcccc aggtacagcc caccctgcgt cgcaaccagg 21420 aacagctcta cagcttcctg gagcgccact cgccctactt ccgcagccac agtgcgcaga 21480 ttaggagcgc cacttctttt tgtcacttga aaaacatgta aaaataatgt actagagaca 21540 ctttcaataa aggcaaatgc ttttatttgt acactctcgg gtgattattt acccccaccc 21600 ttgccgtctg cgccgtttaa aaatcaaagg ggttctgccg cgcatcgcta tgcgccactg 21660 gcagggacac gttgcgatac tggtgtttag tgctccactt aaactcaggc acaaccatcc 21720 gcggcagctc ggtgaagttt tcactccaca ggctgcgcac catcaccaac gcgtttagca 21780 ggtcgggcgc cgatatcttg aagtcgcagt tggggcctcc gccctgcgcg cgcgagttgc 21840 gatacacagg gttgcagcac tggaacacta tcagcgccgg gtggtgcacg ctggccagca 21900 cgctcttgtc ggagatcaga tccgcgtcca ggtcctccgc gttgctcagg gcgaacggag 21960 tcaactttgg tagctgcctt cccaaaaagg gcgcgtgccc aggctttgag ttgcactcgc 22020 accgtagtgg catcaaaagg tgaccgtgcc cggtctgggc gttaggatac agcgcctgca 22080 taaaagcctt gatctgctta aaagccacct gagcctttgc gccttcagag aagaacatgc 22140 cgcaagactt gccggaaaac tgattggccg gacaggccgc gtcgtgcacg cagcaccttg 22200 cgtcggtgtt ggagatctgc accacatttc ggccccaccg gttcttcacg atcttggcct 22260 tgctagactg ctccttcagc gcgcgctgcc cgttttcgct cgtcacatcc atttcaatca 22320 cgtgctcctt atttatcata atgcttccgt gtagacactt aagctcgcct tcgatctcag 22380 cgcagcggtg cagccacaac gcgcagcccg tgggctcgtg atgcttgtag gtcacctctg 22440 caaacgactg caggtacgcc tgcaggaatc gccccatcat cgtcacaaag gtcttgttgc 22500 tggtgaaggt cagctgcaac ccgcggtgct cctcgttcag ccaggtcttg catacggccg 22560 ccagagcttc cacttggtca ggcagtagtt tgaagttcgc ctttagatcg ttatccacgt 22620 ggtacttgtc catcagcgcg cgcgcagcct ccatgccctt ctcccacgca gacacgatcg 22680 gcacactcag cgggttcatc accgtaattt cactttccgc ttcgctgggc tcttcctctt 22740 cctcttgcgt ccgcatacca cgcgccactg ggtcgtcttc attcagccgc cgcactgtgc 22800 gcttacctcc tttgccatgc ttgattagca ccggtgggtt gctgaaaccc accatttgta 22860 gcgccacatc ttctctttct tcctcgctgt ccacgattac ctctggtgat ggcgggcgct 22920 cgggcttggg agaagggcgc ttctttttct tcttgggcgc aatggccaaa tccgccgccg 22980 aggtcgatgg ccgcgggctg ggtgtgcgcg gcaccagcgc gtcttgtgat gagtcttcct 23040 cgtcctcgga ctcgatacgc cgcctcatcc gcttttttgg gggcgcccgg ggaggcggcg 23100 gcgacgggga cggggacgac acgtcctcca tggttggggg acgtcgcgcc gcaccgcgtc 23160 cgcgctcggg ggtggtttcg cgctgctcct cttcccgact ggccatttcc ttctcctata 23220 ggcagaaaaa gatcatggag tcagtcgaga agaaggacag cctaaccgcc ccctctgagt 23280 tcgccaccac cgcctccacc gatgccgcca acgcgcctac caccttcccc gtcgaggcac 23340 ccccgcttga ggaggaggaa gtgattatcg agcaggaccc aggttttgta agcgaagacg 23400 acgaggaccg ctcagtacca acagaggata aaaagcaaga ccaggacaac gcagaggcaa 23460 acgaggaaca agtcgggcgg ggggacgaaa ggcatggcga ctacctagat gtgggagacg 23520 acgtgctgtt gaagcatctg cagcgccagt gcgccattat ctgcgacgcg ttgcaagagc 23580 gcagcgatgt gcccctcgcc atagcggatg tcagccttgc ctacgaacgc cacctattct 23640 caccgcgcgt accccccaaa cgccaagaaa acggcacatg cgagcccaac ccgcgcctca 23700 acttctaccc cgtatttgcc gtgccagagg tgcttgccac ctatcacatc tttttccaaa 23760 actgcaagat acccctatcc tgccgtgcca accgcagccg agcggacaag cagctggcct 23820 tgcggcaggg cgctgtcata cctgatatcg cctcgctcaa cgaagtgcca aaaatctttg 23880 agggtcttgg acgcgacgag aagcgcgcgg caaacgctct gcaacaggaa aacagcgaaa 23940 atgaaagtca ctctggagtg ttggtggaac tcgagggtga caacgcgcgc ctagccgtac 24000 taaaacgcag catcgaggtc acccactttg cctacccggc acttaaccta ccccccaagg 24060 tcatgagcac agtcatgagt gagctgatcg tgcgccgtgc gcagcccctg gagagggatg 24120 caaatttgca agaacaaaca gaggagggcc tacccgcagt tggcgacgag cagctagcgc 24180 gctggcttca aacgcgcgag cctgccgact tggaggagcg acgcaaacta atgatggccg 24240 cagtgctcgt taccgtggag cttgagtgca tgcagcggtt ctttgctgac ccggagatgc 24300 agcgcaagct agaggaaaca ttgcactaca cctttcgaca gggctacgta cgccaggcct 24360 gcaagatctc caacgtggag ctctgcaacc tggtctccta ccttggaatt ttgcacgaaa 24420 accgccttgg gcaaaacgtg cttcattcca cgctcaaggg cgaggcgcgc cgcgactacg 24480 tccgcgactg cgtttactta tttctatgct acacctggca gacggccatg ggcgtttggc 24540 agcagtgctt ggaggagtgc aacctcaagg agctgcagaa actgctaaag caaaacttga 24600 aggacctatg gacggccttc aacgagcgct ccgtggccgc gcacctggcg gacatcattt 24660 tccccgaacg cctgcttaaa accctgcaac agggtctgcc agacttcacc agtcaaagca 24720 tgttgcagaa ctttaggaac tttatcctag agcgctcagg aatcttgccc gccacctgct 24780 gtgcacttcc tagcgacttt gtgcccatta agtaccgcga atgccctccg ccgctttggg 24840 gccactgcta ccttctgcag ctagccaact accttgccta ccactctgac ataatggaag 24900 acgtgagcgg tgacggtcta ctggagtgtc actgtcgctg caacctatgc accccgcacc 24960 gctccctggt ttgcaattcg cagctgctta acgaaagtca aattatcggt acctttgagc 25020 tgcagggtcc ctcgcctgac gaaaagtccg cggctccggg gttgaaactc actccggggc 25080 tgtggacgtc ggcttacctt cgcaaatttg tacctgagga ctaccacgcc cacgagatta 25140 ggttctacga agaccaatcc cgcccgccaa atgcggagct taccgcctgc gtcattaccc 25200 agggccacat tcttggccaa ttgcaagcca tcaacaaagc ccgccaagag tttctgctac 25260 gaaagggacg gggggtttac ttggaccccc agtccggcga ggagctcaac ccaatccccc 25320 cgccgccgca gccctatcag cagcagccgc gggcccttgc ttcccaggat ggcacccaaa 25380 aagaagctgc agctgccgcc gccacccacg gacgaggagg aatactggga cagtcaggca 25440 gaggaggttt tggacgagga ggaggaggac atgatggaag actgggagag cctagacgag 25500 gaagcttccg aggtcgaaga ggtgtcagac gaaacaccgt caccctcggt cgcattcccc 25560 tcgccggcgc cccagaaatc ggcaaccggt tccagcatgg ctacaacctc cgctcctcag 25620 gcgccgccgg cactgcccgt tcgccgaccc aaccgtagat gggacaccac tggaaccagg 25680 gccggtaagt ccaagcagcc gccgccgtta gcccaagagc aacaacagcg ccaaggctac 25740 cgctcatggc gcgggcacaa gaacgccata gttgcttgct tgcaagactg tgggggcaac 25800 atctccttcg cccgccgctt tcttctctac catcacggcg tggccttccc ccgtaacatc 25860 ctgcattact accgtcatct ctacagccca tactgcaccg gcggcagcgg cagcggcagc 25920 aacagcagcg gccacacaga agcaaaggcg accggatagc aagactctga caaagcccaa 25980 gaaatccaca gcggcggcag cagcaggagg aggagcgctg cgtctggcgc ccaacgaacc 26040 cgtatcgacc cgcgagctta gaaacaggat ttttcccact ctgtatgcta tatttcaaca 26100 gagcaggggc caagaacaag agctgaaaat aaaaaacagg tctctgcgat ccctcacccg 26160 cagctgcctg tatcacaaaa gcgaagatca gcttcggcgc acgctggaag acgcggaggc 26220 tctcttcagt aaatactgcg cgctgactct taaggactag tttcgcgccc tttctcaaat 26280 ttaagcgcga aaactacgtc atctccagcg gccacacccg gcgccagcac ctgtcgtcag 26340 cgccattatg agcaaggaaa ttcccacgcc ctacatgtgg agttaccagc cacaaatggg 26400 acttgcggct ggagctgccc aagactactc aacccgaata aactacatga gcgcgggacc 26460 ccacatgata tcccgggtca acggaatccg cgcccaccga aaccgaattc tcttggaaca 26520 ggcggctatt accaccacac ctcgtaataa ccttaatccc cgtagttggc ccgctgccct 26580 ggtgtaccag gaaagtcccg ctcccaccac tgtggtactt cccagagacg cccaggccga 26640 agttcagatg actaactcag gggcgcagct tgcgggcggc tttcgtcaca gggtgcggtc 26700 gcccgggcag ggtataactc acctgacaat cagagggcga ggtattcagc tcaacgacga 26760 gtcggtgagc tcctcgcttg gtctccgtcc ggacgggaca tttcagatcg gcggcgccgg 26820 ccgtccttca ttcacgcctc gtcaggcaat cctaactctg cagacctcgt cctctgagcc 26880 gcgctctgga ggcattggaa ctctgcaatt tattgaggag tttgtgccat cggtctactt 26940 taaccccttc tcgggacctc ccggccacta tccggatcaa tttattccta actttgacgc 27000 ggtaaaggac tcggcggacg gctacgactg aatgttaatt aagttcctgt ccatccgcac 27060 ccactatctt catgttgttg cagatgaagc gcgcaagacc gtctgaagat accttcaacc 27120 ccgtgtatcc atatgacacg gaaaccggtc ctccaactgt gccttttctt actcctccct 27180 ttgtatcccc caatgggttt caagagagtc cccctggggt actctctttg cgcctatccg 27240 aacctctagt tacctccaat ggcatgcttg cgctcaaaat gggcaacggc ctctctctgg 27300 acgaggccgg caaccttacc tcccaaaatg taaccactgt gagcccacct ctcaaaaaaa 27360 ccaagtcaaa cataaacctg gaaatatctg cacccctcac agttacctca gaagccctaa 27420 ctgtggctgc cgccgcacct ctaatggtcg cgggcaacac actcaccatg caatcacagg 27480 ccccgctaac cgtgcacgac tccaaactta gcattgccac ccaaggaccc ctcacagtgt 27540 cagaaggaaa gctagccctg caaacatcag gccccctcac caccaccgat agcagtaccc 27600 ttactatcac tgcctcaccc cctctaacta ctgccactgg tagcttgggc attgacttga 27660 aagagcccat ttatacacaa aatggaaaac taggactaaa gtacggggct cctttgcatg 27720 taacagacga cctaaacact ttgaccgtag caactggtcc aggtgtgact attaataata 27780 cttccttgca aactaaagtt actggagcct tgggttttga ttcacaaggc aatatgcaac 27840 ttaatgtagc aggaggacta aggattgatt ctcaaaacag acgccttata cttgatgtta 27900 gttatccgtt tgatgctcaa aaccaactaa atctaagact aggacagggc cctcttttta 27960 taaactcagc ccacaacttg gatattaact acaacaaagg cctttacttg tttacagctt 28020 caaacaattc caaaaagctt gaggttaacc taagcactgc caaggggttg atgtttgacg 28080 ctacagccat agccattaat gcaggagatg ggcttgaatt tggttcacct aatgcaccaa 28140 acacaaatcc cctcaaaaca aaaattggcc atggcctaga atttgattca aacaaggcta 28200 tggttcctaa actaggaact ggccttagtt ttgacagcac aggtgccatt acagtaggaa 28260 acaaaaataa tgataagcta actttgtgga ccacaccagc tccatctcct aactgtagac 28320 taaatgcaga gaaagatgct aaactcactt tggtcttaac aaaatgtggc agtcaaatac 28380 ttgctacagt ttcagttttg gctgttaaag gcagtttggc tccaatatct ggaacagttc 28440 aaagtgctca tcttattata agatttgacg aaaatggagt gctactaaac aattccttcc 28500 tggacccaga atattggaac tttagaaatg gagatcttac tgaaggcaca gcctatacaa 28560 acgctgttgg atttatgcct aacctatcag cttatccaaa atctcacggt aaaactgcca 28620 aaagtaacat tgtcagtcaa gtttacttaa acggagacaa aactaaacct gtaacactaa 28680 ccattacact aaacggtaca caggaaacag gagacacaac tccaagtgca tactctatgt 28740 cattttcatg ggactggtct ggccacaact acattaatga aatatttgcc acatcctctt 28800 acactttttc atacattgcc caagaataaa gaatcgtttg tgttatgttt caacgtgttt 28860 atttttcaat tgcagaaaat ttcaagtcat ttttcattca gtagtatagc cccaccacca 28920 catagcttat acagatcacc gtaccttaat caaactcaca gaaccctagt attcaacctg 28980 ccacctccct cccaacacac agagtacaca gtcctttctc cccggctggc cttaaaaagc 29040 atcatatcat gggtaacaga catattctta ggtgttatat tccacacggt ttcctgtcga 29100 gccaaacgct catcagtgat attaataaac tccccgggca gctcacttaa gttcatgtcg 29160 ctgtccagct gctgagccac aggctgctgt ccaacttgcg gttgcttaac gggcggcgaa 29220 ggagaagtcc acgcctacat gggggtagag tcataatcgt gcatcaggat agggcggtgg 29280 tgctgcagca gcgcgcgaat aaactgctgc cgccgccgct ccgtcctgca ggaatacaac 29340 atggcagtgg tctcctcagc gatgattcgc accgcccgca gcataaggcg ccttgtcctc 29400 cgggcacagc agcgcaccct gatctcactt aaatcagcac agtaactgca gcacagcacc 29460 acaatattgt tcaaaatccc acagtgcaag gcgctgtatc caaagctcat ggcggggacc 29520 acagaaccca cgtggccatc ataccacaag cgcaggtaga ttaagtggcg acccctcata 29580 aacacgctgg acataaacat tacctctttt ggcatgttgt aattcaccac ctcccggtac 29640 catataaacc tctgattaaa catggcgcca tccaccacca tcctaaacca gctggccaaa 29700 acctgcccgc cggctataca ctgcagggaa ccgggactgg aacaatgaca gtggagagcc 29760 caggactcgt aaccatggat catcatgctc gtcatgatat caatgttggc acaacacagg 29820 cacacgtgca tacacttcct caggattaca agctcctccc gcgttagaac catatcccag 29880 ggaacaaccc attcctgaat cagcgtaaat cccacactgc agggaagacc tcgcacgtaa 29940 ctcacgttgt gcattgtcaa agtgttacat tcgggcagca gcggatgatc ctccagtatg 30000 gtagcgcggg tttctgtctc aaaaggaggt agacgatccc tactgtacgg agtgcgccga 30060 gacaaccgag atcgtgttgg tcgtagtgtc atgccaaatg gaacgccgga cgtagtcata 30120 tttcctgaag caaaaccagg tgcgggcgtg acaaacagat ctgcgtctcc ggtctcgccg 30180 cttagatcgc tctgtgtagt agttgtagta tatccactct ctcaaagcat ccaggcgccc 30240 cctggcttcg ggttctatgt aaactccttc atgcgccgct gccctgataa catccaccac 30300 cgcagaataa gccacaccca gccaacctac acattcgttc tgcgagtcac acacgggagg 30360 agcgggaaga gctggaagaa ccatgttttt ttttttattc caaaagatta tccaaaacct 30420 caaaatgaag atctattaag tgaacgcgct cccctccggt ggcgtggtca aactctacag 30480 ccaaagaaca gataatggca tttgtaagat gttgcacaat ggcttccaaa aggcaaacgg 30540 ccctcacgtc caagtggacg taaaggctaa acccttcagg gtgaatctcc tctataaaca 30600 ttccagcacc ttcaaccatg cccaaataat tctcatctcg ccaccttctc aatatatctc 30660 taagcaaatc ccgaatatta agtccggcca ttgtaaaaat ctgctccaga gcgccctcca 30720 ccttcagcct caagcagcga atcatgattg caaaaattca ggttcctcac agacctgtat 30780 aagattcaaa agcggaacat taacaaaaat accgcgatcc cgtaggtccc ttcgcagggc 30840 cagctgaaca taatcgtgca ggtctgcacg gaccagcgcg gccacttccc cgccaggaac 30900 cttgacaaaa gaacccacac tgattatgac acgcatactc ggagctatgc taaccagcgt 30960 agccccgatg taagctttgt tgcatgggcg gcgatataaa atgcaaggtg ctgctcaaaa 31020 aatcaggcaa agcctcgcgc aaaaaagaaa gcacatcgta gtcatgctca tgcagataaa 31080 ggcaggtaag ctccggaacc accacagaaa aagacaccat ttttctctca aacatgtctg 31140 cgggtttctg cataaacaca aaataaaata acaaaaaaac atttaaacat tagaagcctg 31200 tcttacaaca ggaaaaacaa cccttataag cataagacgg actacggcca tgccggcgtg 31260 accgtaaaaa aactggtcac cgtgattaaa aagcaccacc gacagctcct cggtcatgtc 31320 cggagtcata atgtaagact cggtaaacac atcaggttga ttcatcggtc agtgctaaaa 31380 agcgaccgaa atagcccggg ggaatacata cccgcaggcg tagagacaac attacagccc 31440 ccataggagg tataacaaaa ttaataggag agaaaaacac ataaacacct gaaaaaccct 31500 cctgcctagg caaaatagca ccctcccgct ccagaacaac atacagcgct tcacagcggc 31560 agcctaacag tcagccttac cagtaaaaaa gaaaacctat taaaaaaaca ccactcgaca 31620 cggcaccagc tcaatcagtc acagtgtaaa aaagggccaa gtgcagagcg agtatatata 31680 ggactaaaaa atgacgtaac ggttaaagtc cacaaaaaac acccagaaaa ccgcacgcga 31740 acctacgccc agaaacgaaa gccaaaaaac ccacaacttc ctcaaatcgt cacttccgtt 31800 ttcccacgtt acgtaacttc ccattttaag aaaactacaa ttcccaacac atacaagtta 31860 ctccgcccta aaacctacgt cacccgcccc gttcccacgc cccgcgccac gtcacaaact 31920 ccaccccctc attatcatat tggcttcaat ccaaaataag gtatattatt gatgat 31976 3 32802 DNA Adenovirus 3 catcatcaat aatatacctt attttggatt gaagccaata tgataatgag ggggtggagt 60 ttgtgacgtg gcgcggggcg tgggaacggg gcgggtgacg tagtagtgtg gcggaagtgt 120 gatgttgcaa gtgtggcgga acacatgtaa gcgacggatg tggcaaaagt gacgtttttg 180 gtgtgcgccg gtgtacacag gaagtgacaa ttttcgcgcg gttttaggcg gatgttgtag 240 taaatttggg cgtaaccgag taagatttgg ccattttcgc gggaaaactg aataagagga 300 agtgaaatct gaataatttt gtgttactca tagcgcgtaa tatttgtcta gggccgcggg 360 gactttgacc gtttacgtgg agactcgccc aggtgttttt ctcaggtgtt ttccgcgttc 420 cgggtcaaag ttggcgtttt attattatag tcagctgacg tgtagtgtat ttatacccgg 480 tgagttcctc aagaggccac tcttgagtgc cagcgagtag agttttctcc tccgagccgc 540 tccgacaccg ggactgaaaa tgagacatat tatctgccac ggaggtgtta ttaccgaaga 600 aatggccgcc agtcttttgg accagctgat cgaagaggta ctggctgata atcttccacc 660 tcctagccat tttgaaccac ctacccttca cgaactgtat gatttagacg tgacggcccc 720 cgaagatccc aacgaggagg cggtttcgca gatttttccc gactctgtaa tgttggcggt 780 gcaggaaggg attgacttac tcacttttcc gccggcgccc ggttctccgg agccgcctca 840 cctttcccgg cagcccgagc agccggagca gagagccttg ggtccggttt ctatgccaaa 900 ccttgtaccg gaggtgatcg atcttacctg ccacgaggct ggctttccac ccagtgacga 960 cgaggatgaa gagggtgagg agtttgtgtt agattatgtg gagcaccccg ggcacggttg 1020 caggtcttgt cattatcacc ggaggaatac gggggaccca gatattatgt gttcgctttg 1080 ctatatgagg acctgtggca tgtttgtcta cagtaagtga aaattatggg cagtgggtga 1140 tagagtggtg ggtttggtgt ggtaattttt tttttaattt ttacagtttt gtggtttaaa 1200 gaattttgta ttgtgatttt tttaaaaggt cctgtgtctg aacctgagcc tgagcccgag 1260 ccagaaccgg agcctgcaag acctacccgc cgtcctaaaa tggcgcctgc tatcctgaga 1320 cgcccgacat cacctgtgtc tagagaatgc aatagtagta cggatagctg tgactccggt 1380 ccttctaaca cacctcctga gatacacccg gtggtcccgc tgtgccccat taaaccagtt 1440 gccgtgagag ttggtgggcg tcgccaggct gtggaatgta tcgaggactt gcttaacgag 1500 cctgggcaac ctttggactt gagctgtaaa cgccccaggc cataaggtgt aaacctgtga 1560 ttgcgtgtgt ggttaacgcc tttgtttgct gaatgagttg atgtaagttt aataaagggt 1620 gagataatgt ttaacttgca tggcgtgtta aatggggcgg ggcttaaagg gtatataatg 1680 cgccgtgggc taatcttggt tacatctgac ctcatggagg cttgggagtg tttggaagat 1740 ttttctgctg tgcgtaactt gctggaacag agctctaaca gtacctcttg gttttggagg 1800 tttctgtggg gctcatccca ggcaaagtta gtctgcagaa ttaaggagga ttacaagtgg 1860 gaatttgaag agcttttgaa atcctgtggt gagctgtttg attctttgaa tctgggtcac 1920 caggcgcttt tccaagagaa ggtcatcaag actttggatt tttccacacc ggggcgcgct 1980 gcggctgctg ttgctttttt gagttttata aaggataaat ggagcgaaga aacccatctg 2040 agcggggggt acctgctgga ttttctggcc atgcatctgt ggagagcggt tgtgagacac 2100 aagaatcgcc tgctactgtt gtcttccgtc cgcccggcga taataccgac ggaggagcag 2160 cagcagcagc aggaggaagc caggcggcgg cggcaggagc agagcccatg gaacccgaga 2220 gccggcctgg accctcggga atgaatgttg tacaggtggc tgaactgtat ccagaactga 2280 gacgcatttt gacaattaca gaggatgggc aggggctaaa gggggtaaag agggagcggg 2340 gggcttgtga ggctacagag gaggctagga atctagcttt tagcttaatg accagacacc 2400 gtcctgagtg tattactttt caacagatca aggataattg cgctaatgag cttgatctgc 2460 tggcgcagaa gtattccata gagcagctga ccacttactg gctgcagcca ggggatgatt 2520 ttgaggaggc tattagggta tatgcaaagg tggcacttag gccagattgc aagtacaaga 2580 tcagcaaact tgtaaatatc aggaattgtt gctacatttc tgggaacggg gccgaggtgg 2640 agatagatac ggaggatagg gtggccttta gatgtagcat gataaatatg tggccggggg 2700 tgcttggcat ggacggggtg gttattatga atgtaaggtt tactggcccc aattttagcg 2760 gtacggtttt cctggccaat accaacctta tcctacacgg tgtaagcttc tatgggttta 2820 acaatacctg tgtggaagcc tggaccgatg taagggttcg gggctgtgcc ttttactgct 2880 gctggaaggg ggtggtgtgt cgccccaaaa gcagggcttc aattaagaaa tgcctctttg 2940 aaaggtgtac cttgggtatc ctgtctgagg gtaactccag ggtgcgccac aatgtggcct 3000 ccgactgtgg ttgcttcatg ctagtgaaaa gcgtggctgt gattaagcat aacatggtat 3060 gtggcaactg cgaggacagg gcctctcaga tgctgacctg ctcggacggc aactgtcacc 3120 tgctgaagac cattcacgta gccagccact ctcgcaaggc ctggccagtg tttgagcata 3180 acatactgac ccgctgttcc ttgcatttgg gtaacaggag gggggtgttc ctaccttacc 3240 aatgcaattt gagtcacact aagatattgc ttgagcccga gagcatgtcc aaggtgaacc 3300 tgaacggggt gtttgacatg accatgaaga tctggaaggt gctgaggtac gatgagaccc 3360 gcaccaggtg cagaccctgc gagtgtggcg gtaaacatat taggaaccag cctgtgatgc 3420 tggatgtgac cgaggagctg aggcccgatc acttggtgct ggcctgcacc cgcgctgagt 3480 ttggctctag cgatgaagat acagattgag gtactgaaat gtgtgggcgt ggcttaaggg 3540 tgggaaagaa tatataaggt gggggtctta tgtagttttg tatctgtttt gcagcagccg 3600 ccgccgccat gagcaccaac tcgtttgatg gaagcattgt gagctcatat ttgacaacgc 3660 gcatgccccc atgggccggg gtgcgtcaga atgtgatggg ctccagcatt gatggtcgcc 3720 ccgtcctgcc cgcaaactct actaccttga cctacgagac cgtgtctgga acgccgttgg 3780 agactgcagc ctccgccgcc gcttcagccg ctgcagccac cgcccgcggg attgtgactg 3840 actttgcttt cctgagcccg cttgcaagca gtgcagcttc ccgttcatcc gcccgcgatg 3900 acaagttgac ggctcttttg gcacaattgg attctttgac ccgggaactt aatgtcgttt 3960 ctcagcagct gttggatctg cgccagcagg tttctgccct gaaggcttcc tcccctccca 4020 atgcggttta aaacataaat aaaaaaccag actctgtttg gatttggatc aagcaagtgt 4080 cttgctgtct ttatttaggg gttttgcgcg cgcggtaggc ccgggaccag cggtctcggt 4140 cgttgagggt cctgtgtatt ttttccagga cgtggtaaag gtgactctgg atgttcagat 4200 acatgggcat aagcccgtct ctggggtgga ggtagcacca ctgcagagct tcatgctgcg 4260 gggtggtgtt gtagatgatc cagtcgtagc aggagcgctg ggcgtggtgc ctaaaaatgt 4320 ctttcagtag caagctgatt gccaggggca ggcccttggt gtaagtgttt acaaagcggt 4380 taagctggga tgggtgcata cgtggggata tgagatgcat cttggactgt atttttaggt 4440 tggctatgtt cccagccata tccctccggg gattcatgtt gtgcagaacc accagcacag 4500 tgtatccggt gcacttggga aatttgtcat gtagcttaga aggaaatgcg tggaagaact 4560 tggagacgcc cttgtgacct ccaagatttt ccatgcattc gtccataatg atggcaatgg 4620 gcccacgggc ggcggcctgg gcgaagatat ttctgggatc actaacgtca tagttgtgtt 4680 ccaggatgag atcgtcatag gccattttta caaagcgcgg gcggagggtg ccagactgcg 4740 gtataatggt tccatccggc ccaggggcgt agttaccctc acagatttgc atttcccacg 4800 ctttgagttc agatgggggg atcatgtcta cctgcggggc gatgaagaaa acggtttccg 4860 gggtagggga gatcagctgg gaagaaagca ggttcctgag cagctgcgac ttaccgcagc 4920 cggtgggccc gtaaatcaca cctattaccg ggtgcaactg gtagttaaga gagctgcagc 4980 tgccgtcatc cctgagcagg ggggccactt cgttaagcat gtccctgact cgcatgtttt 5040 ccctgaccaa atccgccaga aggcgctcgc cgcccagcga tagcagttct tgcaaggaag 5100 caaagttttt caacggtttg agaccgtccg ccgtaggcat gcttttgagc gtttgaccaa 5160 gcagttccag gcggtcccac agctcggtca cctgctctac ggcatctcga tccagcatat 5220 ctcctcgttt cgcgggttgg ggcggctttc gctgtacggc agtagtcggt gctcgtccag 5280 acgggccagg gtcatgtctt tccacgggcg cagggtcctc gtcagcgtag tctgggtcac 5340 ggtgaagggg tgcgctccgg gctgcgcgct ggccagggtg cgcttgaggc tggtcctgct 5400 ggtgctgaag cgctgccggt cttcgccctg cgcgtcggcc aggtagcatt tgaccatggt 5460 gtcatagtcc agcccctccg cggcgtggcc cttggcgcgc agcttgccct tggaggaggc 5520 gccgcacgag gggcagtgca gacttttgag ggcgtagagc ttgggcgcga gaaataccga 5580 ttccggggag taggcatccg cgccgcaggc cccgcagacg gtctcgcatt ccacgagcca 5640 ggtgagctct ggccgttcgg ggtcaaaaac caggtttccc ccatgctttt tgatgcgttt 5700 cttacctctg gtttccatga gccggtgtcc acgctcggtg acgaaaaggc tgtccgtgtc 5760 cccgtataca gacttgagag gcctgtcctc gagcggtgtt ccgcggtcct cctcgtatag 5820 aaactcggac cactctgaga caaaggctcg cgtccaggcc agcacgaagg aggctaagtg 5880 ggaggggtag cggtcgttgt ccactagggg gtccactcgc tccagggtgt gaagacacat 5940 gtcgccctct tcggcatcaa ggaaggtgat tggtttgtag gtgtaggcca cgtgaccggg 6000 tgttcctgaa ggggggctat aaaagggggt gggggcgcgt tcgtcctcac tctcttccgc 6060 atcgctgtct gcgagggcca gctgttgggg tgagtactcc ctctgaaaag cgggcatgac 6120 ttctgcgcta agattgtcag tttccaaaaa cgaggaggat ttgatattca cctggcccgc 6180 ggtgatgcct ttgagggtgg ccgcatccat ctggtcagaa aagacaatct ttttgttgtc 6240 aagcttggtg gcaaacgacc cgtagagggc gttggacagc aacttggcga tggagcgcag 6300 ggtttggttt ttgtcgcgat cggcgcgctc cttggccgcg atgtttagct gcacgtattc 6360 gcgcgcaacg caccgccatt cgggaaagac ggtggtgcgc tcgtcgggca ccaggtgcac 6420 gcgccaaccg cggttgtgca gggtgacaag gtcaacgctg gtggctacct ctccgcgtag 6480 gcgctcgttg gtccagcaga ggcggccgcc cttgcgcgag cagaatggcg gtagggggtc 6540 tagctgcgtc tcgtccgggg ggtctgcgtc cacggtaaag accccgggca gcaggcgcgc 6600 gtcgaagtag tctatcttgc atccttgcaa gtctagcgcc tgctgccatg cgcgggcggc 6660 aagcgcgcgc tcgtatgggt tgagtggggg accccatggc atggggtggg tgagcgcgga 6720 ggcgtacatg ccgcaaatgt cgtaaacgta gaggggctct ctgagtattc caagatatgt 6780 agggtagcat cttccaccgc ggatgctggc gcgcacgtaa tcgtatagtt cgtgcgaggg 6840 agcgaggagg tcgggaccga ggttgctacg ggcgggctgc tctgctcgga agactatctg 6900 cctgaagatg gcatgtgagt tggatgatat ggttggacgc tggaagacgt tgaagctggc 6960 gtctgtgaga cctaccgcgt cacgcacgaa ggaggcgtag gagtcgcgca gcttgttgac 7020 cagctcggcg gtgacctgca cgtctagggc gcagtagtcc agggtttcct tgatgatgtc 7080 atacttatcc tgtccctttt ttttccacag ctcgcggttg aggacaaact cttcgcggtc 7140 tttccagtac tcttggatcg gaaacccgtc ggcctccgaa cggtaagagc ctagcatgta 7200 gaactggttg acggcctggt aggcgcagca tcccttttct acgggtagcg cgtatgcctg 7260 cgcggccttc cggagcgagg tgtgggtgag cgcaaaggtg tccctgacca tgactttgag 7320 gtactggtat ttgaagtcag tgtcgtcgca tccgccctgc tcccagagca aaaagtccgt 7380 gcgctttttg gaacgcggat ttggcagggc gaaggtgaca tcgttgaaga gtatctttcc 7440 cgcgcgaggc ataaagttgc gtgtgatgcg gaagggtccc ggcacctcgg aacggttgtt 7500 aattacctgg gcggcgagca cgatctcgtc aaagccgttg atgttgtggc ccacaatgta 7560 aagttccaag aagcgcggga tgcccttgat ggaaggcaat tttttaagtt cctcgtaggt 7620 gagctcttca ggggagctga gcccgtgctc tgaaagggcc cagtctgcaa gatgagggtt 7680 ggaagcgacg aatgagctcc acaggtcacg ggccattagc atttgcaggt ggtcgcgaaa 7740 ggtcctaaac tggcgaccta tggccatttt ttctggggtg atgcagtaga aggtaagcgg 7800 gtcttgttcc cagcggtccc atccaaggtt cgcggctagg tctcgcgcgg cagtcactag 7860 aggctcatct ccgccgaact tcatgaccag catgaagggc acgagctgct tcccaaaggc 7920 ccccatccaa gtataggtct ctacatcgta ggtgacaaag agacgctcgg tgcgaggatg 7980 cgagccgatc gggaagaact ggatctcccg ccaccaattg gaggagtggc tattgatgtg 8040 gtgaaagtag aagtccctgc gacgggccga acactcgtgc tggcttttgt aaaaacgtgc 8100 gcagtactgg cagcggtgca cgggctgtac atcctgcacg aggttgacct gacgaccgcg 8160 cacaaggaag cagagtggga atttgagccc ctcgcctggc gggtttggct ggtggtcttc 8220 tacttcggct gcttgtcctt gaccgtctgg ctgctcgagg ggagttacgg tggatcggac 8280 caccacgccg cgcgagccca aagtccagat gtccgcgcgc ggcggtcgga gcttgatgac 8340 aacatcgcgc agatgggagc tgtccatggt ctggagctcc cgcggcgtca ggtcaggcgg 8400 gagctcctgc aggtttacct cgcatagacg ggtcagggcg cgggctagat ccaggtgata 8460 cctaatttcc aggggctggt tggtggcggc gtcgatggct tgcaagaggc cgcatccccg 8520 cggcgcgact acggtaccgc gcggcgggcg gtgggccgcg ggggtgtcct tggatgatgc 8580 atctaaaagc ggtgacgcgg gcgagccccc ggaggtaggg ggggctccgg acccgccggg 8640 agagggggca ggggcacgtc ggcgccgcgc gcgggcagga gctggtgctg cgcgcgtagg 8700 ttgctggcga acgcgacgac gcggcggttg atctcctgaa tctggcgcct ctgcgtgaag 8760 acgacgggcc cggtgagctt gagcctgaaa gagagttcga cagaatcaat ttcggtgtcg 8820 ttgacggcgg cctggcgcaa aatctcctgc acgtctcctg agttgtcttg ataggcgatc 8880 tcggccatga actgctcgat ctcttcctcc tggagatctc cgcgtccggc tcgctccacg 8940 gtggcggcga ggtcgttgga aatgcgggcc atgagctgcg agaaggcgtt gaggcctccc 9000 tcgttccaga cgcggctgta gaccacgccc ccttcggcat cgcgggcgcg catgaccacc 9060 tgcgcgagat tgagctccac gtgccgggcg aagacggcgt agtttcgcag gcgctgaaag 9120 aggtagttga gggtggtggc ggtgtgttct gccacgaaga agtacataac ccagcgtcgc 9180 aacgtggatt cgttgatatc ccccaaggcc tcaaggcgct ccatggcctc gtagaagtcc 9240 acggcgaagt tgaaaaactg ggagttgcgc gccgacacgg ttaactcctc ctccagaaga 9300 cggatgagct cggcgacagt gtcgcgcacc tcgcgctcaa aggctacagg ggcctcttct 9360 tcttcttcaa tctcctcttc cataagggcc tccccttctt cttcttctgg cggcggtggg 9420 ggagggggga cacggcggcg acgacggcgc accgggaggc ggtcgacaaa gcgctcgatc 9480 atctccccgc ggcgacggcg catggtctcg gtgacggcgc ggccgttctc gcgggggcgc 9540 agttggaaga cgccgcccgt catgtcccgg ttatgggttg gcggggggct gccatgcggc 9600 agggatacgg cgctaacgat gcatctcaac aattgttgtg taggtactcc gccgccgagg 9660 gacctgagcg agtccgcatc gaccggatcg gaaaacctct cgagaaaggc gtctaaccag 9720 tcacagtcgc aaggtaggct gagcaccgtg gcgggcggca gcgggcggcg gtcggggttg 9780 tttctggcgg aggtgctgct gatgatgtaa ttaaagtagg cggtcttgag acggcggatg 9840 gtcgacagaa gcaccatgtc cttgggtccg gcctgctgaa tgcgcaggcg gtcggccatg 9900 ccccaggctt cgttttgaca tcggcgcagg tctttgtagt agtcttgcat gagcctttct 9960 accggcactt cttcttctcc ttcctcttgt cctgcatctc ttgcatctat cgctgcggcg 10020 gcggcggagt ttggccgtag gtggcgccct cttcctccca tgcgtgtgac cccgaagccc 10080 ctcatcggct gaagcagggc taggtcggcg acaacgcgct cggctaatat ggcctgctgc 10140 acctgcgtga gggtagactg gaagtcatcc atgtccacaa agcggtggta tgcgcccgtg 10200 ttgatggtgt aagtgcagtt ggccataacg gaccagttaa cggtctggtg acccggctgc 10260 gagagctcgg tgtacctgag acgcgagtaa gccctcgagt caaatacgta gtcgttgcaa 10320 gtccgcacca ggtactggta tcccaccaaa aagtgcggcg gcggctggcg gtagaggggc 10380 cagcgtaggg tggccggggc tccgggggcg agatcttcca acataaggcg atgatatccg 10440 tagatgtacc tggacatcca ggtgatgccg gcggcggtgg tggaggcgcg cggaaagtcg 10500 cggacgcggt tccagatgtt gcgcagcggc aaaaagtgct ccatggtcgg gacgctctgg 10560 ccggtcaggc gcgcgcaatc gttgacgctc tagaccgtgc aaaaggagag cctgtaagcg 10620 ggcactcttc cgtggtctgg tggataaatt cgcaagggta tcatggcgga cgaccggggt 10680 tcgagccccg tatccggccg tccgccgtga tccatgcggt taccgcccgc gtgtcgaacc 10740 caggtgtgcg acgtcagaca acgggggagt gctccttttg gcttccttcc aggcgcggcg 10800 gctgctgcgc tagctttttt ggccactggc cgcgcgcagc gtaagcggtt aggctggaaa 10860 gcgaaagcat taagtggctc gctccctgta gccggagggt tattttccaa gggttgagtc 10920 gcgggacccc cggttcgagt ctcggaccgg ccggactgcg gcgaacgggg gtttgcctcc 10980 ccgtcatgca agaccccgct tgcaaattcc tccggaaaca gggacgagcc ccttttttgc 11040 ttttcccaga tgcatccggt gctgcggcag atgcgccccc ctcctcagca gcggcaagag 11100 caagagcagc ggcagacatg cagggcaccc tcccctcctc ctaccgcgtc aggaggggcg 11160 acatccgcgg ttgacgcggc agcagatggt gattacgaac ccccgcggcg ccgggcccgg 11220 cactacctgg acttggagga gggcgagggc ctggcgcggc taggagcgcc ctctcctgag 11280 cggtacccaa gggtgcagct gaagcgtgat acgcgtgagg cgtacgtgcc gcggcagaac 11340 ctgtttcgcg accgcgaggg agaggagccc gaggagatgc gggatcgaaa gttccacgca 11400 gggcgcgagc tgcggcatgg cctgaatcgc gagcggttgc tgcgcgagga ggactttgag 11460 cccgacgcgc gaaccgggat tagtcccgcg cgcgcacacg tggcggccgc cgacctggta 11520 accgcatacg agcagacggt gaaccaggag attaactttc aaaaaagctt taacaaccac 11580 gtgcgtacgc ttgtggcgcg cgaggaggtg gctataggac tgatgcatct gtgggacttt 11640 gtaagcgcgc tggagcaaaa cccaaatagc aagccgctca tggcgcagct gttccttata 11700 gtgcagcaca gcagggacaa cgaggcattc agggatgcgc tgctaaacat agtagagccc 11760 gagggccgct ggctgctcga tttgataaac atcctgcaga gcatagtggt gcaggagcgc 11820 agcttgagcc tggctgacaa ggtggccgcc atcaactatt ccatgcttag cctgggcaag 11880 ttttacgccc gcaagatata ccatacccct tacgttccca tagacaagga ggtaaagatc 11940 gaggggttct acatgcgcat ggcgctgaag gtgcttacct tgagcgacga cctgggcgtt 12000 tatcgcaacg agcgcatcca caaggccgtg agcgtgagcc ggcggcgcga gctcagcgac 12060 cgcgagctga tgcacagcct gcaaagggcc ctggctggca cgggcagcgg cgatagagag 12120 gccgagtcct actttgacgc gggcgctgac ctgcgctggg ccccaagccg acgcgccctg 12180 gaggcagctg gggccggacc tgggctggcg gtggcacccg cgcgcgctgg caacgtcggc 12240 ggcgtggagg aatatgacga ggacgatgag tacgagccag aggacggcga gtactaagcg 12300 gtgatgtttc tgatcagatg atgcaagacg caacggaccc ggcggtgcgg gcggcgctgc 12360 agagccagcc gtccggcctt aactccacgg acgactggcg ccaggtcatg gaccgcatca 12420 tgtcgctgac tgcgcgcaat cctgacgcgt tccggcagca gccgcaggcc aaccggctct 12480 ccgcaattct ggaagcggtg gtcccggcgc gcgcaaaccc cacgcacgag aaggtgctgg 12540 cgatcgtaaa cgcgctggcc gaaaacaggg ccatccggcc cgacgaggcc ggcctggtct 12600 acgacgcgct gcttcagcgc gtggctcgtt acaacagcgg caacgtgcag accaacctgg 12660 accggctggt gggggatgtg cgcgaggccg tggcgcagcg tgagcgcgcg cagcagcagg 12720 gcaacctggg ctccatggtt gcactaaacg ccttcctgag tacacagccc gccaacgtgc 12780 cgcggggaca ggaggactac accaactttg tgagcgcact gcggctaatg gtgactgaga 12840 caccgcaaag tgaggtgtac cagtctgggc cagactattt tttccagacc agtagacaag 12900 gcctgcagac cgtaaacctg agccaggctt tcaaaaactt gcaggggctg tggggggtgc 12960 gggctcccac aggcgaccgc gcgaccgtgt ctagcttgct gacgcccaac tcgcgcctgt 13020 tgctgctgct aatagcgccc ttcacggaca gtggcagcgt gtcccgggac acatacctag 13080 gtcacttgct gacactgtac cgcgaggcca taggtcaggc gcatgtggac gagcatactt 13140 tccaggagat tacaagtgtc agccgcgcgc tggggcagga ggacacgggc agcctggagg 13200 caaccctaaa ctacctgctg accaaccggc ggcagaagat cccctcgttg cacagtttaa 13260 acagcgagga ggagcgcatt ttgcgctacg tgcagcagag cgtgagcctt aacctgatgc 13320 gcgacggggt aacgcccagc gtggcgctgg acatgaccgc gcgcaacatg gaaccgggca 13380 tgtatgcctc aaaccggccg tttatcaacc gcctaatgga ctacttgcat cgcgcggccg 13440 ccgtgaaccc cgagtatttc accaatgcca tcttgaaccc gcactggcta ccgccccctg 13500 gtttctacac cgggggattc gaggtgcccg agggtaacga tggattcctc tgggacgaca 13560 tagacgacag cgtgttttcc ccgcaaccgc agaccctgct agagttgcaa cagcgcgagc 13620 aggcagaggc ggcgctgcga aaggaaagct tccgcaggcc aagcagcttg tccgatctag 13680 gcgctgcggc cccgcggtca gatgctagta gcccatttcc aagcttgata gggtctctta 13740 ccagcactcg caccacccgc ccgcgcctgc tgggcgagga ggagtaccta aacaactcgc 13800 tgctgcagcc gcagcgcgaa aaaaacctgc ctccggcatt tcccaacaac gggatagaga 13860 gcctagtgga caagatgagt agatggaaga cgtacgcgca ggagcacagg gacgtgccag 13920 gcccgcgccc gcccacccgt cgtcaaaggc acgaccgtca gcggggtctg gtgtgggagg 13980 acgatgactc ggcagacgac agcagcgtcc tggatttggg agggagtggc aacccgtttg 14040 cgcaccttcg ccccaggctg gggagaatgt tttaaaaaaa aaaaagcatg atgcaaaata 14100 aaaaactcac caaggccatg gcaccgagcg ttggttttct tgtattcccc ttagtatgcg 14160 gcgcgcggcg atgtatgagg aaggtcctcc tccctcctac gagagtgtgg tgagcgcggc 14220 gccagtggcg gcggcgctgg gttctccctt cgatgctccc ctggacccgc cgtttgtgcc 14280 tccgcggtac ctgcggccta ccggggggag aaacagcatc cgttactctg agttggcacc 14340 cctattcgac accacccgtg tgtacctggt ggacaacaag tcaacggatg tggcatccct 14400 gaactaccag aacgaccaca gcaactttct gaccacggtc attcaaaaca atgactacag 14460 cccgggggag gcaagcacac agaccatcaa tcttgacgac cggtcgcact ggggcggcga 14520 cctgaaaacc atcctgcata ccaacatgcc aaatgtgaac gagttcatgt ttaccaataa 14580 gtttaaggcg cgggtgatgg tgtcgcgctt gcctactaag gacaatcagg tggagctgaa 14640 atacgagtgg gtggagttca cgctgcccga gggcaactac tccgagacca tgaccataga 14700 ccttatgaac aacgcgatcg tggagcacta cttgaaagtg ggcagacaga acggggttct 14760 ggaaagcgac atcggggtaa agtttgacac ccgcaacttc agactggggt ttgaccccgt 14820 cactggtctt gtcatgcctg gggtatatac aaacgaagcc ttccatccag acatcatttt 14880 gctgccagga tgcggggtgg acttcaccca cagccgcctg agcaacttgt tgggcatccg 14940 caagcggcaa cccttccagg agggctttag gatcacctac gatgatctgg agggtggtaa 15000 cattcccgca ctgttggatg tggacgccta ccaggcgagc ttgaaagatg acaccgaaca 15060 gggcgggggt ggcgcaggcg gcagcaacag cagtggcagc ggcgcggaag agaactccaa 15120 cgcggcagcc gcggcaatgc agccggtgga ggacatgaac gatcatgcca ttcgcggcga 15180 cacctttgcc acacgggctg aggagaagcg cgctgaggcc gaagcagcgg ccgaagctgc 15240 cgcccccgct gcgcaacccg aggtcgagaa gcctcagaag aaaccggtga tcaaacccct 15300 gacagaggac agcaagaaac gcagttacaa cctaataagc aatgacagca ccttcaccca 15360 gtaccgcagc tggtaccttg catacaacta cggcgaccct cagaccggaa tccgctcatg 15420 gaccctgctt tgcactcctg acgtaacctg cggctcggag caggtctact ggtcgttgcc 15480 agacatgatg caagaccccg tgaccttccg ctccacgcgc cagatcagca actttccggt 15540 ggtgggcgcc gagctgttgc ccgtgcactc caagagcttc tacaacgacc aggccgtcta 15600 ctcccaactc atccgccagt ttacctctct gacccacgtg ttcaatcgct ttcccgagaa 15660 ccagattttg gcgcgcccgc cagcccccac catcaccacc gtcagtgaaa acgttcctgc 15720 tctcacagat cacgggacgc taccgctgcg caacagcatc ggaggagtcc agcgagtgac 15780 cattactgac gccagacgcc gcacctgccc ctacgtttac aaggccctgg gcatagtctc 15840 gccgcgcgtc ctatcgagcc gcactttttg agcaagcatg tccatcctta tatcgcccag 15900 caataacaca ggctggggcc tgcgcttccc aagcaagatg tttggcgggg ccaagaagcg 15960 ctccgaccaa cacccagtgc gcgtgcgcgg gcactaccgc gcgccctggg gcgcgcacaa 16020 acgcggccgc actgggcgca ccaccgtcga tgacgccatc gacgcggtgg tggaggaggc 16080 gcgcaactac acgcccacgc cgccaccagt gtccacagtg gacgcggcca ttcagaccgt 16140 ggtgcgcgga gcccggcgct atgctaaaat gaagagacgg cggaggcgcg tagcacgtcg 16200 ccaccgccgc cgacccggca ctgccgccca acgcgcggcg gcggccctgc ttaaccgcgc 16260 acgtcgcacc ggccgacggg cggccatgcg ggccgctcga aggctggccg cgggtattgt 16320 cactgtgccc cccaggtcca ggcgacgagc ggccgccgca gcagccgcgg ccattagtgc 16380 tatgactcag ggtcgcaggg gcaacgtgta ttgggtgcgc gactcggtta gcggcctgcg 16440 cgtgcccgtg cgcacccgcc ccccgcgcaa ctagattgca agaaaaaact acttagactc 16500 gtactgttgt atgtatccag cggcggcggc gcgcaacgaa gctatgtcca agcgcaaaat 16560 caaagaagag atgctccagg tcatcgcgcc ggagatctat ggccccccga agaaggaaga 16620 gcaggattac aagccccgaa agctaaagcg ggtcaaaaag aaaaagaaag atgatgatga 16680 tgaacttgac gacgaggtgg aactgctgca cgctaccgcg cccaggcgac gggtacagtg 16740 gaaaggtcga cgcgtaaaac gtgttttgcg acccggcacc accgtagtct ttacgcccgg 16800 tgagcgctcc acccgcacct acaagcgcgt gtatgatgag gtgtacggcg acgaggacct 16860 gcttgagcag gccaacgagc gcctcgggga gtttgcctac ggaaagcggc ataaggacat 16920 gctggcgttg ccgctggacg agggcaaccc aacacctagc ctaaagcccg taacactgca 16980 gcaggtgctg cccgcgcttg caccgtccga agaaaagcgc ggcctaaagc gcgagtctgg 17040 tgacttggca cccaccgtgc agctgatggt acccaagcgc cagcgactgg aagatgtctt 17100 ggaaaaaatg accgtggaac ctgggctgga gcccgaggtc cgcgtgcggc caatcaagca 17160 ggtggcgccg ggactgggcg tgcagaccgt ggacgttcag atacccacta ccagtagcac 17220 cagtattgcc accgccacag agggcatgga gacacaaacg tccccggttg cctcagcggt 17280 ggcggatgcc gcggtgcagg cggtcgctgc ggccgcgtcc aagacctcta cggaggtgca 17340 aacggacccg tggatgtttc gcgtttcagc cccccggcgc ccgcgcggtt cgaggaagta 17400 cggcgccgcc agcgcgctac tgcccgaata tgccctacat ccttccattg cgcctacccc 17460 cggctatcgt ggctacacct accgccccag aagacgagca actacccgac gccgaaccac 17520 cactggaacc cgccgccgcc gtcgccgtcg ccagcccgtg ctggccccga tttccgtgcg 17580 cagggtggct cgcgaaggag gcaggaccct ggtgctgcca acagcgcgct accaccccag 17640 catcgtttaa aagccggtct ttgtggttct tgcagatatg gccctcacct gccgcctccg 17700 tttcccggtg ccgggattcc gaggaagaat gcaccgtagg aggggcatgg ccggccacgg 17760 cctgacgggc ggcatgcgtc gtgcgcacca ccggcggcgg cgcgcgtcgc accgtcgcat 17820 gcgcggcggt atcctgcccc tccttattcc actgatcgcc gcggcgattg gcgccgtgcc 17880 cggaattgca tccgtggcct tgcaggcgca gagacactga ttaaaaacaa gttgcatgtg 17940 gaaaaatcaa aataaaaagt ctggactctc acgctcgctt ggtcctgtaa ctattttgta 18000 gaatggaaga catcaacttt gcgtctctgg ccccgcgaca cggctcgcgc ccgttcatgg 18060 gaaactggca agatatcggc accagcaata tgagcggtgg cgccttcagc tggggctcgc 18120 tgtggagcgg cattaaaaat ttcggttcca ccgttaagaa ctatggcagc aaggcctgga 18180 acagcagcac aggccagatg ctgagggata agttgaaaga gcaaaatttc caacaaaagg 18240 tggtagatgg cctggcctct ggcattagcg gggtggtgga cctggccaac caggcagtgc 18300 aaaataagat taacagtaag cttgatcccc gccctcccgt agaggagcct ccaccggccg 18360 tggagacagt gtctccagag gggcgtggcg aaaagcgtcc gcgccccgac agggaagaaa 18420 ctctggtgac gcaaatagac gagcctccct cgtacgagga ggcactaaag caaggcctgc 18480 ccaccacccg tcccatcgcg cccatggcta ccggagtgct gggccagcac acacccgtaa 18540 cgctggacct gcctcccccc gccgacaccc agcagaaacc tgtgctgcca ggcccgaccg 18600 ccgttgttgt aacccgtcct agccgcgcgt ccctgcgccg cgccgccagc ggtccgcgat 18660 cgttgcggcc cgtagccagt ggcaactggc aaagcacact gaacagcatc gtgggtctgg 18720 gggtgcaatc cctgaagcgc cgacgatgct tctgaatagc taacgtgtcg tatgtgtgtc 18780 atgtatgcgt ccatgtcgcc gccagaggag ctgctgagcc gccgcgcgcc cgctttccaa 18840 gatggctacc ccttcgatga tgccgcagtg gtcttacatg cacatctcgg gccaggacgc 18900 ctcggagtac ctgagccccg ggctggtgca gtttgcccgc gccaccgaga cgtacttcag 18960 cctgaataac aagtttagaa accccacggt ggcgcctacg cacgacgtga ccacagaccg 19020 gtcccagcgt ttgacgctgc ggttcatccc tgtggaccgt gaggatactg cgtactcgta 19080 caaggcgcgg ttcaccctag ctgtgggtga taaccgtgtg ctggacatgg cttccacgta 19140 ctttgacatc cgcggcgtgc tggacagggg ccctactttt aagccctact ctggcactgc 19200 ctacaacgcc ctggctccca agggtgcccc aaatccttgc gaatgggatg aagctgctac 19260 tgctcttgaa ataaacctag aagaagagga cgatgacaac gaagacgaag tagacgagca 19320 agctgagcag caaaaaactc acgtatttgg gcaggcgcct tattctggta taaatattac 19380 aaaggagggt attcaaatag gtgtcgaagg tcaaacacct aaatatgccg ataaaacatt 19440 tcaacctgaa cctcaaatag gagaatctca gtggtacgaa actgaaatta atcatgcagc 19500 tgggagagtc cttaaaaaga ctaccccaat gaaaccatgt tacggttcat atgcaaaacc 19560 cacaaatgaa aatggagggc aaggcattct tgtaaagcaa caaaatggaa agctagaaag 19620 tcaagtggaa atgcaatttt tctcaactac tgaggcgacc gcaggcaatg gtgataactt 19680 gactcctaaa gtggtattgt acagtgaaga tgtagatata gaaaccccag acactcatat 19740 ttcttacatg cccactatta aggaaggtaa ctcacgagaa ctaatgggcc aacaatctat 19800 gcccaacagg cctaattaca ttgcttttag ggacaatttt attggtctaa tgtattacaa 19860 cagcacgggt aatatgggtg ttctggcggg ccaagcatcg cagttgaatg ctgttgtaga 19920 tttgcaagac agaaacacag agctttcata ccagcttttg cttgattcca ttggtgatag 19980 aaccaggtac ttttctatgt ggaatcaggc tgttgacagc tatgatccag atgttagaat 20040 tattgaaaat catggaactg aagatgaact tccaaattac tgctttccac tgggaggtgt 20100 gattaataca gagactctta ccaaggtaaa acctaaaaca ggtcaggaaa atggatggga 20160 aaaagatgct acagaatttt cagataaaaa tgaaataaga gttggaaata attttgccat 20220 ggaaatcaat ctaaatgcca acctgtggag aaatttcctg tactccaaca tagcgctgta 20280 tttgcccgac aagctaaagt acagtccttc caacgtaaaa atttctgata acccaaacac 20340 ctacgactac atgaacaagc gagtggtggc tcccgggtta gtggactgct acattaacct 20400 tggagcacgc tggtcccttg actatatgga caacgtcaac ccatttaacc accaccgcaa 20460 tgctggcctg cgctaccgct caatgttgct gggcaatggt cgctatgtgc ccttccacat 20520 ccaggtgcct cagaagttct ttgccattaa aaacctcctt ctcctgccgg gctcatacac 20580 ctacgagtgg aacttcagga aggatgttaa catggttctg cagagctccc taggaaatga 20640 cctaagggtt gacggagcca gcattaagtt tgatagcatt tgcctttacg ccaccttctt 20700 ccccatggcc cacaacaccg cctccacgct tgaggccatg cttagaaacg acaccaacga 20760 ccagtccttt aacgactatc tctccgccgc caacatgctc taccctatac ccgccaacgc 20820 taccaacgtg cccatatcca tcccctcccg caactgggcg gctttccgcg gctgggcctt 20880 cacgcgcctt aagactaagg aaaccccatc actgggctcg ggctacgacc cttattacac 20940 ctactctggc tctataccct acctagatgg aaccttttac ctcaaccaca cctttaagaa 21000 ggtggccatt acctttgact cttctgtcag ctggcctggc aatgaccgcc tgcttacccc 21060 caacgagttt gaaattaagc gctcagttga cggggagggt tacaacgttg cccagtgtaa 21120 catgaccaaa gactggttcc tggtacaaat gctagctaac tacaacattg gctaccaggg 21180 cttctatatc ccagagagct acaaggaccg catgtactcc ttctttagaa acttccagcc 21240 catgagccgt caggtggtgg atgatactaa atacaaggac taccaacagg tgggcatcct 21300 acaccaacac aacaactctg gatttgttgg ctaccttgcc cccaccatgc gcgaaggaca 21360 ggcctaccct gctaacttcc cctatccgct tataggcaag accgcagttg acagcattac 21420 ccagaaaaag tttctttgcg atcgcaccct ttggcgcatc ccattctcca gtaactttat 21480 gtccatgggc gcactcacag acctgggcca aaaccttctc tacgccaact ccgcccacgc 21540 gctagacatg acttttgagg tggatcccat ggacgagccc acccttcttt atgttttgtt 21600 tgaagtcttt gacgtggtcc gtgtgcaccg gccgcaccgc ggcgtcatcg aaaccgtgta 21660 cctgcgcacg cccttctcgg ccggcaacgc cacaacataa agaagcaagc aacatcaaca 21720 acagctgccg ccatgggctc cagtgagcag gaactgaaag ccattgtcaa agatcttggt 21780 tgtgggccat attttttggg cacctatgac aagcgctttc caggctttgt ttctccacac 21840 aagctcgcct gcgccatagt caatacggcc ggtcgcgaga ctgggggcgt acactggatg 21900 gcctttgcct ggaacccgca ctcaaaaaca tgctacctct ttgagccctt tggcttttct 21960 gaccagcgac tcaagcaggt ttaccagttt gagtacgagt cactcctgcg ccgtagcgcc 22020 attgcttctt cccccgaccg ctgtataacg ctggaaaagt ccacccaaag cgtacagggg 22080 cccaactcgg ccgcctgtgg actattctgc tgcatgtttc tccacgcctt tgccaactgg 22140 ccccaaactc ccatggatca caaccccacc atgaacctta ttaccggggt acccaactcc 22200 atgctcaaca gtccccaggt acagcccacc ctgcgtcgca accaggaaca gctctacagc 22260 ttcctggagc gccactcgcc ctacttccgc agccacagtg cgcagattag gagcgccact 22320 tctttttgtc acttgaaaaa catgtaaaaa taatgtacta gagacacttt caataaaggc 22380 aaatgctttt atttgtacac tctcgggtga ttatttaccc ccacccttgc cgtctgcgcc 22440 gtttaaaaat caaaggggtt ctgccgcgca tcgctatgcg ccactggcag ggacacgttg 22500 cgatactggt gtttagtgct ccacttaaac tcaggcacaa ccatccgcgg cagctcggtg 22560 aagttttcac tccacaggct gcgcaccatc accaacgcgt ttagcaggtc gggcgccgat 22620 atcttgaagt cgcagttggg gcctccgccc tgcgcgcgcg agttgcgata cacagggttg 22680 cagcactgga acactatcag cgccgggtgg tgcacgctgg ccagcacgct cttgtcggag 22740 atcagatccg cgtccaggtc ctccgcgttg ctcagggcga acggagtcaa ctttggtagc 22800 tgccttccca aaaagggcgc gtgcccaggc tttgagttgc actcgcaccg tagtggcatc 22860 aaaaggtgac cgtgcccggt ctgggcgtta ggatacagcg cctgcataaa agccttgatc 22920 tgcttaaaag ccacctgagc ctttgcgcct tcagagaaga acatgccgca agacttgccg 22980 gaaaactgat tggccggaca ggccgcgtcg tgcacgcagc accttgcgtc ggtgttggag 23040 atctgcacca catttcggcc ccaccggttc ttcacgatct tggccttgct agactgctcc 23100 ttcagcgcgc gctgcccgtt ttcgctcgtc acatccattt caatcacgtg ctccttattt 23160 atcataatgc ttccgtgtag acacttaagc tcgccttcga tctcagcgca gcggtgcagc 23220 cacaacgcgc agcccgtggg ctcgtgatgc ttgtaggtca cctctgcaaa cgactgcagg 23280 tacgcctgca ggaatcgccc catcatcgtc acaaaggtct tgttgctggt gaaggtcagc 23340 tgcaacccgc ggtgctcctc gttcagccag gtcttgcata cggccgccag agcttccact 23400 tggtcaggca gtagtttgaa gttcgccttt agatcgttat ccacgtggta cttgtccatc 23460 agcgcgcgcg cagcctccat gcccttctcc cacgcagaca cgatcggcac actcagcggg 23520 ttcatcaccg taatttcact ttccgcttcg ctgggctctt cctcttcctc ttgcgtccgc 23580 ataccacgcg ccactgggtc gtcttcattc agccgccgca ctgtgcgctt acctcctttg 23640 ccatgcttga ttagcaccgg tgggttgctg aaacccacca tttgtagcgc cacatcttct 23700 ctttcttcct cgctgtccac gattacctct ggtgatggcg ggcgctcggg cttgggagaa 23760 gggcgcttct ttttcttctt gggcgcaatg gccaaatccg ccgccgaggt cgatggccgc 23820 gggctgggtg tgcgcggcac cagcgcgtct tgtgatgagt cttcctcgtc ctcggactcg 23880 atacgccgcc tcatccgctt ttttgggggc gcccggggag gcggcggcga cggggacggg 23940 gacgacacgt cctccatggt tgggggacgt cgcgccgcac cgcgtccgcg ctcgggggtg 24000 gtttcgcgct gctcctcttc ccgactggcc atttccttct cctataggca gaaaaagatc 24060 atggagtcag tcgagaagaa ggacagccta accgccccct ctgagttcgc caccaccgcc 24120 tccaccgatg ccgccaacgc gcctaccacc ttccccgtcg aggcaccccc gcttgaggag 24180 gaggaagtga ttatcgagca ggacccaggt tttgtaagcg aagacgacga ggaccgctca 24240 gtaccaacag aggataaaaa gcaagaccag gacaacgcag aggcaaacga ggaacaagtc 24300 gggcgggggg acgaaaggca tggcgactac ctagatgtgg gagacgacgt gctgttgaag 24360 catctgcagc gccagtgcgc cattatctgc gacgcgttgc aagagcgcag cgatgtgccc 24420 ctcgccatag cggatgtcag ccttgcctac gaacgccacc tattctcacc gcgcgtaccc 24480 cccaaacgcc aagaaaacgg cacatgcgag cccaacccgc gcctcaactt ctaccccgta 24540 tttgccgtgc cagaggtgct tgccacctat cacatctttt tccaaaactg caagataccc 24600 ctatcctgcc gtgccaaccg cagccgagcg gacaagcagc tggccttgcg gcagggcgct 24660 gtcatacctg atatcgcctc gctcaacgaa gtgccaaaaa tctttgaggg tcttggacgc 24720 gacgagaagc gcgcggcaaa cgctctgcaa caggaaaaca gcgaaaatga aagtcactct 24780 ggagtgttgg tggaactcga gggtgacaac gcgcgcctag ccgtactaaa acgcagcatc 24840 gaggtcaccc actttgccta cccggcactt aacctacccc ccaaggtcat gagcacagtc 24900 atgagtgagc tgatcgtgcg ccgtgcgcag cccctggaga gggatgcaaa tttgcaagaa 24960 caaacagagg agggcctacc cgcagttggc gacgagcagc tagcgcgctg gcttcaaacg 25020 cgcgagcctg ccgacttgga ggagcgacgc aaactaatga tggccgcagt gctcgttacc 25080 gtggagcttg agtgcatgca gcggttcttt gctgacccgg agatgcagcg caagctagag 25140 gaaacattgc actacacctt tcgacagggc tacgtacgcc aggcctgcaa gatctccaac 25200 gtggagctct gcaacctggt ctcctacctt ggaattttgc acgaaaaccg ccttgggcaa 25260 aacgtgcttc attccacgct caagggcgag gcgcgccgcg actacgtccg cgactgcgtt 25320 tacttatttc tatgctacac ctggcagacg gccatgggcg tttggcagca gtgcttggag 25380 gagtgcaacc tcaaggagct gcagaaactg ctaaagcaaa acttgaagga cctatggacg 25440 gccttcaacg agcgctccgt ggccgcgcac ctggcggaca tcattttccc cgaacgcctg 25500 cttaaaaccc tgcaacaggg tctgccagac ttcaccagtc aaagcatgtt gcagaacttt 25560 aggaacttta tcctagagcg ctcaggaatc ttgcccgcca cctgctgtgc acttcctagc 25620 gactttgtgc ccattaagta ccgcgaatgc cctccgccgc tttggggcca ctgctacctt 25680 ctgcagctag ccaactacct tgcctaccac tctgacataa tggaagacgt gagcggtgac 25740 ggtctactgg agtgtcactg tcgctgcaac ctatgcaccc cgcaccgctc cctggtttgc 25800 aattcgcagc tgcttaacga aagtcaaatt atcggtacct ttgagctgca gggtccctcg 25860 cctgacgaaa agtccgcggc tccggggttg aaactcactc cggggctgtg gacgtcggct 25920 taccttcgca aatttgtacc tgaggactac cacgcccacg agattaggtt ctacgaagac 25980 caatcccgcc cgccaaatgc ggagcttacc gcctgcgtca ttacccaggg ccacattctt 26040 ggccaattgc aagccatcaa caaagcccgc caagagtttc tgctacgaaa gggacggggg 26100 gtttacttgg acccccagtc cggcgaggag ctcaacccaa tccccccgcc gccgcagccc 26160 tatcagcagc agccgcgggc ccttgcttcc caggatggca cccaaaaaga agctgcagct 26220 gccgccgcca cccacggacg aggaggaata ctgggacagt caggcagagg aggttttgga 26280 cgaggaggag gaggacatga tggaagactg ggagagccta gacgaggaag cttccgaggt 26340 cgaagaggtg tcagacgaaa caccgtcacc ctcggtcgca ttcccctcgc cggcgcccca 26400 gaaatcggca accggttcca gcatggctac aacctccgct cctcaggcgc cgccggcact 26460 gcccgttcgc cgacccaacc gtagatggga caccactgga accagggccg gtaagtccaa 26520 gcagccgccg ccgttagccc aagagcaaca acagcgccaa ggctaccgct catggcgcgg 26580 gcacaagaac gccatagttg cttgcttgca agactgtggg ggcaacatct ccttcgcccg 26640 ccgctttctt ctctaccatc acggcgtggc cttcccccgt aacatcctgc attactaccg 26700 tcatctctac agcccatact gcaccggcgg cagcggcagc ggcagcaaca gcagcggcca 26760 cacagaagca aaggcgaccg gatagcaaga ctctgacaaa gcccaagaaa tccacagcgg 26820 cggcagcagc aggaggagga gcgctgcgtc tggcgcccaa cgaacccgta tcgacccgcg 26880 agcttagaaa caggattttt cccactctgt atgctatatt tcaacagagc aggggccaag 26940 aacaagagct gaaaataaaa aacaggtctc tgcgatccct cacccgcagc tgcctgtatc 27000 acaaaagcga agatcagctt cggcgcacgc tggaagacgc ggaggctctc ttcagtaaat 27060 actgcgcgct gactcttaag gactagtttc gcgccctttc tcaaatttaa gcgcgaaaac 27120 tacgtcatct ccagcggcca cacccggcgc cagcacctgt cgtcagcgcc attatgagca 27180 aggaaattcc cacgccctac atgtggagtt accagccaca aatgggactt gcggctggag 27240 ctgcccaaga ctactcaacc cgaataaact acatgagcgc gggaccccac atgatatccc 27300 gggtcaacgg aatccgcgcc caccgaaacc gaattctctt ggaacaggcg gctattacca 27360 ccacacctcg taataacctt aatccccgta gttggcccgc tgccctggtg taccaggaaa 27420 gtcccgctcc caccactgtg gtacttccca gagacgccca ggccgaagtt cagatgacta 27480 actcaggggc gcagcttgcg ggcggctttc gtcacagggt gcggtcgccc gggcagggta 27540 taactcacct gacaatcaga gggcgaggta ttcagctcaa cgacgagtcg gtgagctcct 27600 cgcttggtct ccgtccggac gggacatttc agatcggcgg cgccggccgt ccttcattca 27660 cgcctcgtca ggcaatccta actctgcaga cctcgtcctc tgagccgcgc tctggaggca 27720 ttggaactct gcaatttatt gaggagtttg tgccatcggt ctactttaac cccttctcgg 27780 gacctcccgg ccactatccg gatcaattta ttcctaactt tgacgcggta aaggactcgg 27840 cggacggcta cgactgaatg ttaattaagt tcctgtccat ccgcacccac tatcttcatg 27900 ttgttgcaga tgaagcgcgc aagaccgtct gaagatacct tcaaccccgt gtatccatat 27960 gacacggaaa ccggtcctcc aactgtgcct tttcttactc ctccctttgt atcccccaat 28020 gggtttcaag agagtccccc tggggtactc tctttgcgcc tatccgaacc tctagttacc 28080 tccaatggca tgcttgcgct caaaatgggc aacggcctct ctctggacga ggccggcaac 28140 cttacctccc aaaatgtaac cactgtgagc ccacctctca aaaaaaccaa gtcaaacata 28200 aacctggaaa tatctgcacc cctcacagtt acctcagaag ccctaactgt ggctgccgcc 28260 gcacctctaa tggtcgcggg caacacactc accatgcaat cacaggcccc gctaaccgtg 28320 cacgactcca aacttagcat tgccacccaa ggacccctca cagtgtcaga aggaaagcta 28380 gccctgcaaa catcaggccc cctcaccacc accgatagca gtacccttac tatcactgcc 28440 tcaccccctc taactactgc cactggtagc ttgggcattg acttgaaaga gcccatttat 28500 acacaaaatg gaaaactagg actaaagtac ggggctcctt tgcatgtaac agacgaccta 28560 aacactttga ccgtagcaac tggtccaggt gtgactatta ataatacttc cttgcaaact 28620 aaagttactg gagccttggg ttttgattca caaggcaata tgcaacttaa tgtagcagga 28680 ggactaagga ttgattctca aaacagacgc cttatacttg atgttagtta tccgtttgat 28740 gctcaaaacc aactaaatct aagactagga cagggccctc tttttataaa ctcagcccac 28800 aacttggata ttaactacaa caaaggcctt tacttgttta cagcttcaaa caattccaaa 28860 aagcttgagg ttaacctaag cactgccaag gggttgatgt ttgacgctac agccatagcc 28920 attaatgcag gagatgggct tgaatttggt tcacctaatg caccaaacac aaatcccctc 28980 aaaacaaaaa ttggccatgg cctagaattt gattcaaaca aggctatggt tcctaaacta 29040 ggaactggcc ttagttttga cagcacaggt gccattacag taggaaacaa aaataatgat 29100 aagctaactt tgtggaccac accagctcca tctcctaact gtagactaaa tgcagagaaa 29160 gatgctaaac tcactttggt cttaacaaaa tgtggcagtc aaatacttgc tacagtttca 29220 gttttggctg ttaaaggcag tttggctcca atatctggaa cagttcaaag tgctcatctt 29280 attataagat ttgacgaaaa tggagtgcta ctaaacaatt ccttcctgga cccagaatat 29340 tggaacttta gaaatggaga tcttactgaa ggcacagcct atacaaacgc tgttggattt 29400 atgcctaacc tatcagctta tccaaaatct cacggtaaaa ctgccaaaag taacattgtc 29460 agtcaagttt acttaaacgg agacaaaact aaacctgtaa cactaaccat tacactaaac 29520 ggtacacagg aaacaggaga cacaactcca agtgcatact ctatgtcatt ttcatgggac 29580 tggtctggcc acaactacat taatgaaata tttgccacat cctcttacac tttttcatac 29640 attgcccaag aataaagaat cgtttgtgtt atgtttcaac gtgtttattt ttcaattgca 29700 gaaaatttca agtcattttt cattcagtag tatagcccca ccaccacata gcttatacag 29760 atcaccgtac cttaatcaaa ctcacagaac cctagtattc aacctgccac ctccctccca 29820 acacacagag tacacagtcc tttctccccg gctggcctta aaaagcatca tatcatgggt 29880 aacagacata ttcttaggtg ttatattcca cacggtttcc tgtcgagcca aacgctcatc 29940 agtgatatta ataaactccc cgggcagctc acttaagttc atgtcgctgt ccagctgctg 30000 agccacaggc tgctgtccaa cttgcggttg cttaacgggc ggcgaaggag aagtccacgc 30060 ctacatgggg gtagagtcat aatcgtgcat caggataggg cggtggtgct gcagcagcgc 30120 gcgaataaac tgctgccgcc gccgctccgt cctgcaggaa tacaacatgg cagtggtctc 30180 ctcagcgatg attcgcaccg cccgcagcat aaggcgcctt gtcctccggg cacagcagcg 30240 caccctgatc tcacttaaat cagcacagta actgcagcac agcaccacaa tattgttcaa 30300 aatcccacag tgcaaggcgc tgtatccaaa gctcatggcg gggaccacag aacccacgtg 30360 gccatcatac cacaagcgca ggtagattaa gtggcgaccc ctcataaaca cgctggacat 30420 aaacattacc tcttttggca tgttgtaatt caccacctcc cggtaccata taaacctctg 30480 attaaacatg gcgccatcca ccaccatcct aaaccagctg gccaaaacct gcccgccggc 30540 tatacactgc agggaaccgg gactggaaca atgacagtgg agagcccagg actcgtaacc 30600 atggatcatc atgctcgtca tgatatcaat gttggcacaa cacaggcaca cgtgcataca 30660 cttcctcagg attacaagct cctcccgcgt tagaaccata tcccagggaa caacccattc 30720 ctgaatcagc gtaaatccca cactgcaggg aagacctcgc acgtaactca cgttgtgcat 30780 tgtcaaagtg ttacattcgg gcagcagcgg atgatcctcc agtatggtag cgcgggtttc 30840 tgtctcaaaa ggaggtagac gatccctact gtacggagtg cgccgagaca accgagatcg 30900 tgttggtcgt agtgtcatgc caaatggaac gccggacgta gtcatatttc ctgaagcaaa 30960 accaggtgcg ggcgtgacaa acagatctgc gtctccggtc tcgccgctta gatcgctctg 31020 tgtagtagtt gtagtatatc cactctctca aagcatccag gcgccccctg gcttcgggtt 31080 ctatgtaaac tccttcatgc gccgctgccc tgataacatc caccaccgca gaataagcca 31140 cacccagcca acctacacat tcgttctgcg agtcacacac gggaggagcg ggaagagctg 31200 gaagaaccat gttttttttt ttattccaaa agattatcca aaacctcaaa atgaagatct 31260 attaagtgaa cgcgctcccc tccggtggcg tggtcaaact ctacagccaa agaacagata 31320 atggcatttg taagatgttg cacaatggct tccaaaaggc aaacggccct cacgtccaag 31380 tggacgtaaa ggctaaaccc ttcagggtga atctcctcta taaacattcc agcaccttca 31440 accatgccca aataattctc atctcgccac cttctcaata tatctctaag caaatcccga 31500 atattaagtc cggccattgt aaaaatctgc tccagagcgc cctccacctt cagcctcaag 31560 cagcgaatca tgattgcaaa aattcaggtt cctcacagac ctgtataaga ttcaaaagcg 31620 gaacattaac aaaaataccg cgatcccgta ggtcccttcg cagggccagc tgaacataat 31680 cgtgcaggtc tgcacggacc agcgcggcca cttccccgcc aggaaccttg acaaaagaac 31740 ccacactgat tatgacacgc atactcggag ctatgctaac cagcgtagcc ccgatgtaag 31800 ctttgttgca tgggcggcga tataaaatgc aaggtgctgc tcaaaaaatc aggcaaagcc 31860 tcgcgcaaaa aagaaagcac atcgtagtca tgctcatgca gataaaggca ggtaagctcc 31920 ggaaccacca cagaaaaaga caccattttt ctctcaaaca tgtctgcggg tttctgcata 31980 aacacaaaat aaaataacaa aaaaacattt aaacattaga agcctgtctt acaacaggaa 32040 aaacaaccct tataagcata agacggacta cggccatgcc ggcgtgaccg taaaaaaact 32100 ggtcaccgtg attaaaaagc accaccgaca gctcctcggt catgtccgga gtcataatgt 32160 aagactcggt aaacacatca ggttgattca tcggtcagtg ctaaaaagcg accgaaatag 32220 cccgggggaa tacatacccg caggcgtaga gacaacatta cagcccccat aggaggtata 32280 acaaaattaa taggagagaa aaacacataa acacctgaaa aaccctcctg cctaggcaaa 32340 atagcaccct cccgctccag aacaacatac agcgcttcac agcggcagcc taacagtcag 32400 ccttaccagt aaaaaagaaa acctattaaa aaaacaccac tcgacacggc accagctcaa 32460 tcagtcacag tgtaaaaaag ggccaagtgc agagcgagta tatataggac taaaaaatga 32520 cgtaacggtt aaagtccaca aaaaacaccc agaaaaccgc acgcgaacct acgcccagaa 32580 acgaaagcca aaaaacccac aacttcctca aatcgtcact tccgttttcc cacgttacgt 32640 aacttcccat tttaagaaaa ctacaattcc caacacatac aagttactcc gccctaaaac 32700 ctacgtcacc cgccccgttc ccacgccccg cgccacgtca caaactccac cccctcatta 32760 tcatattggc ttcaatccaa aataaggtat attattgatg at 32802 4 35935 DNA adenovirus 4 catcatcaat aatatacctt attttggatt gaagccaata tgataatgag ggggtggagt 60 ttgtgacgtg gcgcggggcg tgggaacggg gcgggtgacg tagtagtgtg gcggaagtgt 120 gatgttgcaa gtgtggcgga acacatgtaa gcgacggatg tggcaaaagt gacgtttttg 180 gtgtgcgccg gtgtacacag gaagtgacaa ttttcgcgcg gttttaggcg gatgttgtag 240 taaatttggg cgtaaccgag taagatttgg ccattttcgc gggaaaactg aataagagga 300 agtgaaatct gaataatttt gtgttactca tagcgcgtaa tatttgtcta gggccgcggg 360 gactttgacc gtttacgtgg agactcgccc aggtgttttt ctcaggtgtt ttccgcgttc 420 cgggtcaaag ttggcgtttt attattatag tcagctgacg tgtagtgtat ttatacccgg 480 tgagttcctc aagaggccac tcttgagtgc cagcgagtag agttttctcc tccgagccgc 540 tccgacaccg ggactgaaaa tgagacatat tatctgccac ggaggtgtta ttaccgaaga 600 aatggccgcc agtcttttgg accagctgat cgaagaggta ctggctgata atcttccacc 660 tcctagccat tttgaaccac ctacccttca cgaactgtat gatttagacg tgacggcccc 720 cgaagatccc aacgaggagg cggtttcgca gatttttccc gactctgtaa tgttggcggt 780 gcaggaaggg attgacttac tcacttttcc gccggcgccc ggttctccgg agccgcctca 840 cctttcccgg cagcccgagc agccggagca gagagccttg ggtccggttt ctatgccaaa 900 ccttgtaccg gaggtgatcg atcttacctg ccacgaggct ggctttccac ccagtgacga 960 cgaggatgaa gagggtgagg agtttgtgtt agattatgtg gagcaccccg ggcacggttg 1020 caggtcttgt cattatcacc ggaggaatac gggggaccca gatattatgt gttcgctttg 1080 ctatatgagg acctgtggca tgtttgtcta cagtaagtga aaattatggg cagtgggtga 1140 tagagtggtg ggtttggtgt ggtaattttt tttttaattt ttacagtttt gtggtttaaa 1200 gaattttgta ttgtgatttt tttaaaaggt cctgtgtctg aacctgagcc tgagcccgag 1260 ccagaaccgg agcctgcaag acctacccgc cgtcctaaaa tggcgcctgc tatcctgaga 1320 cgcccgacat cacctgtgtc tagagaatgc aatagtagta cggatagctg tgactccggt 1380 ccttctaaca cacctcctga gatacacccg gtggtcccgc tgtgccccat taaaccagtt 1440 gccgtgagag ttggtgggcg tcgccaggct gtggaatgta tcgaggactt gcttaacgag 1500 cctgggcaac ctttggactt gagctgtaaa cgccccaggc cataaggtgt aaacctgtga 1560 ttgcgtgtgt ggttaacgcc tttgtttgct gaatgagttg atgtaagttt aataaagggt 1620 gagataatgt ttaacttgca tggcgtgtta aatggggcgg ggcttaaagg gtatataatg 1680 cgccgtgggc taatcttggt tacatctgac ctcatggagg cttgggagtg tttggaagat 1740 ttttctgctg tgcgtaactt gctggaacag agctctaaca gtacctcttg gttttggagg 1800 tttctgtggg gctcatccca ggcaaagtta gtctgcagaa ttaaggagga ttacaagtgg 1860 gaatttgaag agcttttgaa atcctgtggt gagctgtttg attctttgaa tctgggtcac 1920 caggcgcttt tccaagagaa ggtcatcaag actttggatt tttccacacc ggggcgcgct 1980 gcggctgctg ttgctttttt gagttttata aaggataaat ggagcgaaga aacccatctg 2040 agcggggggt acctgctgga ttttctggcc atgcatctgt ggagagcggt tgtgagacac 2100 aagaatcgcc tgctactgtt gtcttccgtc cgcccggcga taataccgac ggaggagcag 2160 cagcagcagc aggaggaagc caggcggcgg cggcaggagc agagcccatg gaacccgaga 2220 gccggcctgg accctcggga atgaatgttg tacaggtggc tgaactgtat ccagaactga 2280 gacgcatttt gacaattaca gaggatgggc aggggctaaa gggggtaaag agggagcggg 2340 gggcttgtga ggctacagag gaggctagga atctagcttt tagcttaatg accagacacc 2400 gtcctgagtg tattactttt caacagatca aggataattg cgctaatgag cttgatctgc 2460 tggcgcagaa gtattccata gagcagctga ccacttactg gctgcagcca ggggatgatt 2520 ttgaggaggc tattagggta tatgcaaagg tggcacttag gccagattgc aagtacaaga 2580 tcagcaaact tgtaaatatc aggaattgtt gctacatttc tgggaacggg gccgaggtgg 2640 agatagatac ggaggatagg gtggccttta gatgtagcat gataaatatg tggccggggg 2700 tgcttggcat ggacggggtg gttattatga atgtaaggtt tactggcccc aattttagcg 2760 gtacggtttt cctggccaat accaacctta tcctacacgg tgtaagcttc tatgggttta 2820 acaatacctg tgtggaagcc tggaccgatg taagggttcg gggctgtgcc ttttactgct 2880 gctggaaggg ggtggtgtgt cgccccaaaa gcagggcttc aattaagaaa tgcctctttg 2940 aaaggtgtac cttgggtatc ctgtctgagg gtaactccag ggtgcgccac aatgtggcct 3000 ccgactgtgg ttgcttcatg ctagtgaaaa gcgtggctgt gattaagcat aacatggtat 3060 gtggcaactg cgaggacagg gcctctcaga tgctgacctg ctcggacggc aactgtcacc 3120 tgctgaagac cattcacgta gccagccact ctcgcaaggc ctggccagtg tttgagcata 3180 acatactgac ccgctgttcc ttgcatttgg gtaacaggag gggggtgttc ctaccttacc 3240 aatgcaattt gagtcacact aagatattgc ttgagcccga gagcatgtcc aaggtgaacc 3300 tgaacggggt gtttgacatg accatgaaga tctggaaggt gctgaggtac gatgagaccc 3360 gcaccaggtg cagaccctgc gagtgtggcg gtaaacatat taggaaccag cctgtgatgc 3420 tggatgtgac cgaggagctg aggcccgatc acttggtgct ggcctgcacc cgcgctgagt 3480 ttggctctag cgatgaagat acagattgag gtactgaaat gtgtgggcgt ggcttaaggg 3540 tgggaaagaa tatataaggt gggggtctta tgtagttttg tatctgtttt gcagcagccg 3600 ccgccgccat gagcaccaac tcgtttgatg gaagcattgt gagctcatat ttgacaacgc 3660 gcatgccccc atgggccggg gtgcgtcaga atgtgatggg ctccagcatt gatggtcgcc 3720 ccgtcctgcc cgcaaactct actaccttga cctacgagac cgtgtctgga acgccgttgg 3780 agactgcagc ctccgccgcc gcttcagccg ctgcagccac cgcccgcggg attgtgactg 3840 actttgcttt cctgagcccg cttgcaagca gtgcagcttc ccgttcatcc gcccgcgatg 3900 acaagttgac ggctcttttg gcacaattgg attctttgac ccgggaactt aatgtcgttt 3960 ctcagcagct gttggatctg cgccagcagg tttctgccct gaaggcttcc tcccctccca 4020 atgcggttta aaacataaat aaaaaaccag actctgtttg gatttggatc aagcaagtgt 4080 cttgctgtct ttatttaggg gttttgcgcg cgcggtaggc ccgggaccag cggtctcggt 4140 cgttgagggt cctgtgtatt ttttccagga cgtggtaaag gtgactctgg atgttcagat 4200 acatgggcat aagcccgtct ctggggtgga ggtagcacca ctgcagagct tcatgctgcg 4260 gggtggtgtt gtagatgatc cagtcgtagc aggagcgctg ggcgtggtgc ctaaaaatgt 4320 ctttcagtag caagctgatt gccaggggca ggcccttggt gtaagtgttt acaaagcggt 4380 taagctggga tgggtgcata cgtggggata tgagatgcat cttggactgt atttttaggt 4440 tggctatgtt cccagccata tccctccggg gattcatgtt gtgcagaacc accagcacag 4500 tgtatccggt gcacttggga aatttgtcat gtagcttaga aggaaatgcg tggaagaact 4560 tggagacgcc cttgtgacct ccaagatttt ccatgcattc gtccataatg atggcaatgg 4620 gcccacgggc ggcggcctgg gcgaagatat ttctgggatc actaacgtca tagttgtgtt 4680 ccaggatgag atcgtcatag gccattttta caaagcgcgg gcggagggtg ccagactgcg 4740 gtataatggt tccatccggc ccaggggcgt agttaccctc acagatttgc atttcccacg 4800 ctttgagttc agatgggggg atcatgtcta cctgcggggc gatgaagaaa acggtttccg 4860 gggtagggga gatcagctgg gaagaaagca ggttcctgag cagctgcgac ttaccgcagc 4920 cggtgggccc gtaaatcaca cctattaccg ggtgcaactg gtagttaaga gagctgcagc 4980 tgccgtcatc cctgagcagg ggggccactt cgttaagcat gtccctgact cgcatgtttt 5040 ccctgaccaa atccgccaga aggcgctcgc cgcccagcga tagcagttct tgcaaggaag 5100 caaagttttt caacggtttg agaccgtccg ccgtaggcat gcttttgagc gtttgaccaa 5160 gcagttccag gcggtcccac agctcggtca cctgctctac ggcatctcga tccagcatat 5220 ctcctcgttt cgcgggttgg ggcggctttc gctgtacggc agtagtcggt gctcgtccag 5280 acgggccagg gtcatgtctt tccacgggcg cagggtcctc gtcagcgtag tctgggtcac 5340 ggtgaagggg tgcgctccgg gctgcgcgct ggccagggtg cgcttgaggc tggtcctgct 5400 ggtgctgaag cgctgccggt cttcgccctg cgcgtcggcc aggtagcatt tgaccatggt 5460 gtcatagtcc agcccctccg cggcgtggcc cttggcgcgc agcttgccct tggaggaggc 5520 gccgcacgag gggcagtgca gacttttgag ggcgtagagc ttgggcgcga gaaataccga 5580 ttccggggag taggcatccg cgccgcaggc cccgcagacg gtctcgcatt ccacgagcca 5640 ggtgagctct ggccgttcgg ggtcaaaaac caggtttccc ccatgctttt tgatgcgttt 5700 cttacctctg gtttccatga gccggtgtcc acgctcggtg acgaaaaggc tgtccgtgtc 5760 cccgtataca gacttgagag gcctgtcctc gagcggtgtt ccgcggtcct cctcgtatag 5820 aaactcggac cactctgaga caaaggctcg cgtccaggcc agcacgaagg aggctaagtg 5880 ggaggggtag cggtcgttgt ccactagggg gtccactcgc tccagggtgt gaagacacat 5940 gtcgccctct tcggcatcaa ggaaggtgat tggtttgtag gtgtaggcca cgtgaccggg 6000 tgttcctgaa ggggggctat aaaagggggt gggggcgcgt tcgtcctcac tctcttccgc 6060 atcgctgtct gcgagggcca gctgttgggg tgagtactcc ctctgaaaag cgggcatgac 6120 ttctgcgcta agattgtcag tttccaaaaa cgaggaggat ttgatattca cctggcccgc 6180 ggtgatgcct ttgagggtgg ccgcatccat ctggtcagaa aagacaatct ttttgttgtc 6240 aagcttggtg gcaaacgacc cgtagagggc gttggacagc aacttggcga tggagcgcag 6300 ggtttggttt ttgtcgcgat cggcgcgctc cttggccgcg atgtttagct gcacgtattc 6360 gcgcgcaacg caccgccatt cgggaaagac ggtggtgcgc tcgtcgggca ccaggtgcac 6420 gcgccaaccg cggttgtgca gggtgacaag gtcaacgctg gtggctacct ctccgcgtag 6480 gcgctcgttg gtccagcaga ggcggccgcc cttgcgcgag cagaatggcg gtagggggtc 6540 tagctgcgtc tcgtccgggg ggtctgcgtc cacggtaaag accccgggca gcaggcgcgc 6600 gtcgaagtag tctatcttgc atccttgcaa gtctagcgcc tgctgccatg cgcgggcggc 6660 aagcgcgcgc tcgtatgggt tgagtggggg accccatggc atggggtggg tgagcgcgga 6720 ggcgtacatg ccgcaaatgt cgtaaacgta gaggggctct ctgagtattc caagatatgt 6780 agggtagcat cttccaccgc ggatgctggc gcgcacgtaa tcgtatagtt cgtgcgaggg 6840 agcgaggagg tcgggaccga ggttgctacg ggcgggctgc tctgctcgga agactatctg 6900 cctgaagatg gcatgtgagt tggatgatat ggttggacgc tggaagacgt tgaagctggc 6960 gtctgtgaga cctaccgcgt cacgcacgaa ggaggcgtag gagtcgcgca gcttgttgac 7020 cagctcggcg gtgacctgca cgtctagggc gcagtagtcc agggtttcct tgatgatgtc 7080 atacttatcc tgtccctttt ttttccacag ctcgcggttg aggacaaact cttcgcggtc 7140 tttccagtac tcttggatcg gaaacccgtc ggcctccgaa cggtaagagc ctagcatgta 7200 gaactggttg acggcctggt aggcgcagca tcccttttct acgggtagcg cgtatgcctg 7260 cgcggccttc cggagcgagg tgtgggtgag cgcaaaggtg tccctgacca tgactttgag 7320 gtactggtat ttgaagtcag tgtcgtcgca tccgccctgc tcccagagca aaaagtccgt 7380 gcgctttttg gaacgcggat ttggcagggc gaaggtgaca tcgttgaaga gtatctttcc 7440 cgcgcgaggc ataaagttgc gtgtgatgcg gaagggtccc ggcacctcgg aacggttgtt 7500 aattacctgg gcggcgagca cgatctcgtc aaagccgttg atgttgtggc ccacaatgta 7560 aagttccaag aagcgcggga tgcccttgat ggaaggcaat tttttaagtt cctcgtaggt 7620 gagctcttca ggggagctga gcccgtgctc tgaaagggcc cagtctgcaa gatgagggtt 7680 ggaagcgacg aatgagctcc acaggtcacg ggccattagc atttgcaggt ggtcgcgaaa 7740 ggtcctaaac tggcgaccta tggccatttt ttctggggtg atgcagtaga aggtaagcgg 7800 gtcttgttcc cagcggtccc atccaaggtt cgcggctagg tctcgcgcgg cagtcactag 7860 aggctcatct ccgccgaact tcatgaccag catgaagggc acgagctgct tcccaaaggc 7920 ccccatccaa gtataggtct ctacatcgta ggtgacaaag agacgctcgg tgcgaggatg 7980 cgagccgatc gggaagaact ggatctcccg ccaccaattg gaggagtggc tattgatgtg 8040 gtgaaagtag aagtccctgc gacgggccga acactcgtgc tggcttttgt aaaaacgtgc 8100 gcagtactgg cagcggtgca cgggctgtac atcctgcacg aggttgacct gacgaccgcg 8160 cacaaggaag cagagtggga atttgagccc ctcgcctggc gggtttggct ggtggtcttc 8220 tacttcggct gcttgtcctt gaccgtctgg ctgctcgagg ggagttacgg tggatcggac 8280 caccacgccg cgcgagccca aagtccagat gtccgcgcgc ggcggtcgga gcttgatgac 8340 aacatcgcgc agatgggagc tgtccatggt ctggagctcc cgcggcgtca ggtcaggcgg 8400 gagctcctgc aggtttacct cgcatagacg ggtcagggcg cgggctagat ccaggtgata 8460 cctaatttcc aggggctggt tggtggcggc gtcgatggct tgcaagaggc cgcatccccg 8520 cggcgcgact acggtaccgc gcggcgggcg gtgggccgcg ggggtgtcct tggatgatgc 8580 atctaaaagc ggtgacgcgg gcgagccccc ggaggtaggg ggggctccgg acccgccggg 8640 agagggggca ggggcacgtc ggcgccgcgc gcgggcagga gctggtgctg cgcgcgtagg 8700 ttgctggcga acgcgacgac gcggcggttg atctcctgaa tctggcgcct ctgcgtgaag 8760 acgacgggcc cggtgagctt gagcctgaaa gagagttcga cagaatcaat ttcggtgtcg 8820 ttgacggcgg cctggcgcaa aatctcctgc acgtctcctg agttgtcttg ataggcgatc 8880 tcggccatga actgctcgat ctcttcctcc tggagatctc cgcgtccggc tcgctccacg 8940 gtggcggcga ggtcgttgga aatgcgggcc atgagctgcg agaaggcgtt gaggcctccc 9000 tcgttccaga cgcggctgta gaccacgccc ccttcggcat cgcgggcgcg catgaccacc 9060 tgcgcgagat tgagctccac gtgccgggcg aagacggcgt agtttcgcag gcgctgaaag 9120 aggtagttga gggtggtggc ggtgtgttct gccacgaaga agtacataac ccagcgtcgc 9180 aacgtggatt cgttgatatc ccccaaggcc tcaaggcgct ccatggcctc gtagaagtcc 9240 acggcgaagt tgaaaaactg ggagttgcgc gccgacacgg ttaactcctc ctccagaaga 9300 cggatgagct cggcgacagt gtcgcgcacc tcgcgctcaa aggctacagg ggcctcttct 9360 tcttcttcaa tctcctcttc cataagggcc tccccttctt cttcttctgg cggcggtggg 9420 ggagggggga cacggcggcg acgacggcgc accgggaggc ggtcgacaaa gcgctcgatc 9480 atctccccgc ggcgacggcg catggtctcg gtgacggcgc ggccgttctc gcgggggcgc 9540 agttggaaga cgccgcccgt catgtcccgg ttatgggttg gcggggggct gccatgcggc 9600 agggatacgg cgctaacgat gcatctcaac aattgttgtg taggtactcc gccgccgagg 9660 gacctgagcg agtccgcatc gaccggatcg gaaaacctct cgagaaaggc gtctaaccag 9720 tcacagtcgc aaggtaggct gagcaccgtg gcgggcggca gcgggcggcg gtcggggttg 9780 tttctggcgg aggtgctgct gatgatgtaa ttaaagtagg cggtcttgag acggcggatg 9840 gtcgacagaa gcaccatgtc cttgggtccg gcctgctgaa tgcgcaggcg gtcggccatg 9900 ccccaggctt cgttttgaca tcggcgcagg tctttgtagt agtcttgcat gagcctttct 9960 accggcactt cttcttctcc ttcctcttgt cctgcatctc ttgcatctat cgctgcggcg 10020 gcggcggagt ttggccgtag gtggcgccct cttcctccca tgcgtgtgac cccgaagccc 10080 ctcatcggct gaagcagggc taggtcggcg acaacgcgct cggctaatat ggcctgctgc 10140 acctgcgtga gggtagactg gaagtcatcc atgtccacaa agcggtggta tgcgcccgtg 10200 ttgatggtgt aagtgcagtt ggccataacg gaccagttaa cggtctggtg acccggctgc 10260 gagagctcgg tgtacctgag acgcgagtaa gccctcgagt caaatacgta gtcgttgcaa 10320 gtccgcacca ggtactggta tcccaccaaa aagtgcggcg gcggctggcg gtagaggggc 10380 cagcgtaggg tggccggggc tccgggggcg agatcttcca acataaggcg atgatatccg 10440 tagatgtacc tggacatcca ggtgatgccg gcggcggtgg tggaggcgcg cggaaagtcg 10500 cggacgcggt tccagatgtt gcgcagcggc aaaaagtgct ccatggtcgg gacgctctgg 10560 ccggtcaggc gcgcgcaatc gttgacgctc tagaccgtgc aaaaggagag cctgtaagcg 10620 ggcactcttc cgtggtctgg tggataaatt cgcaagggta tcatggcgga cgaccggggt 10680 tcgagccccg tatccggccg tccgccgtga tccatgcggt taccgcccgc gtgtcgaacc 10740 caggtgtgcg acgtcagaca acgggggagt gctccttttg gcttccttcc aggcgcggcg 10800 gctgctgcgc tagctttttt ggccactggc cgcgcgcagc gtaagcggtt aggctggaaa 10860 gcgaaagcat taagtggctc gctccctgta gccggagggt tattttccaa gggttgagtc 10920 gcgggacccc cggttcgagt ctcggaccgg ccggactgcg gcgaacgggg gtttgcctcc 10980 ccgtcatgca agaccccgct tgcaaattcc tccggaaaca gggacgagcc ccttttttgc 11040 ttttcccaga tgcatccggt gctgcggcag atgcgccccc ctcctcagca gcggcaagag 11100 caagagcagc ggcagacatg cagggcaccc tcccctcctc ctaccgcgtc aggaggggcg 11160 acatccgcgg ttgacgcggc agcagatggt gattacgaac ccccgcggcg ccgggcccgg 11220 cactacctgg acttggagga gggcgagggc ctggcgcggc taggagcgcc ctctcctgag 11280 cggtacccaa gggtgcagct gaagcgtgat acgcgtgagg cgtacgtgcc gcggcagaac 11340 ctgtttcgcg accgcgaggg agaggagccc gaggagatgc gggatcgaaa gttccacgca 11400 gggcgcgagc tgcggcatgg cctgaatcgc gagcggttgc tgcgcgagga ggactttgag 11460 cccgacgcgc gaaccgggat tagtcccgcg cgcgcacacg tggcggccgc cgacctggta 11520 accgcatacg agcagacggt gaaccaggag attaactttc aaaaaagctt taacaaccac 11580 gtgcgtacgc ttgtggcgcg cgaggaggtg gctataggac tgatgcatct gtgggacttt 11640 gtaagcgcgc tggagcaaaa cccaaatagc aagccgctca tggcgcagct gttccttata 11700 gtgcagcaca gcagggacaa cgaggcattc agggatgcgc tgctaaacat agtagagccc 11760 gagggccgct ggctgctcga tttgataaac atcctgcaga gcatagtggt gcaggagcgc 11820 agcttgagcc tggctgacaa ggtggccgcc atcaactatt ccatgcttag cctgggcaag 11880 ttttacgccc gcaagatata ccatacccct tacgttccca tagacaagga ggtaaagatc 11940 gaggggttct acatgcgcat ggcgctgaag gtgcttacct tgagcgacga cctgggcgtt 12000 tatcgcaacg agcgcatcca caaggccgtg agcgtgagcc ggcggcgcga gctcagcgac 12060 cgcgagctga tgcacagcct gcaaagggcc ctggctggca cgggcagcgg cgatagagag 12120 gccgagtcct actttgacgc gggcgctgac ctgcgctggg ccccaagccg acgcgccctg 12180 gaggcagctg gggccggacc tgggctggcg gtggcacccg cgcgcgctgg caacgtcggc 12240 ggcgtggagg aatatgacga ggacgatgag tacgagccag aggacggcga gtactaagcg 12300 gtgatgtttc tgatcagatg atgcaagacg caacggaccc ggcggtgcgg gcggcgctgc 12360 agagccagcc gtccggcctt aactccacgg acgactggcg ccaggtcatg gaccgcatca 12420 tgtcgctgac tgcgcgcaat cctgacgcgt tccggcagca gccgcaggcc aaccggctct 12480 ccgcaattct ggaagcggtg gtcccggcgc gcgcaaaccc cacgcacgag aaggtgctgg 12540 cgatcgtaaa cgcgctggcc gaaaacaggg ccatccggcc cgacgaggcc ggcctggtct 12600 acgacgcgct gcttcagcgc gtggctcgtt acaacagcgg caacgtgcag accaacctgg 12660 accggctggt gggggatgtg cgcgaggccg tggcgcagcg tgagcgcgcg cagcagcagg 12720 gcaacctggg ctccatggtt gcactaaacg ccttcctgag tacacagccc gccaacgtgc 12780 cgcggggaca ggaggactac accaactttg tgagcgcact gcggctaatg gtgactgaga 12840 caccgcaaag tgaggtgtac cagtctgggc cagactattt tttccagacc agtagacaag 12900 gcctgcagac cgtaaacctg agccaggctt tcaaaaactt gcaggggctg tggggggtgc 12960 gggctcccac aggcgaccgc gcgaccgtgt ctagcttgct gacgcccaac tcgcgcctgt 13020 tgctgctgct aatagcgccc ttcacggaca gtggcagcgt gtcccgggac acatacctag 13080 gtcacttgct gacactgtac cgcgaggcca taggtcaggc gcatgtggac gagcatactt 13140 tccaggagat tacaagtgtc agccgcgcgc tggggcagga ggacacgggc agcctggagg 13200 caaccctaaa ctacctgctg accaaccggc ggcagaagat cccctcgttg cacagtttaa 13260 acagcgagga ggagcgcatt ttgcgctacg tgcagcagag cgtgagcctt aacctgatgc 13320 gcgacggggt aacgcccagc gtggcgctgg acatgaccgc gcgcaacatg gaaccgggca 13380 tgtatgcctc aaaccggccg tttatcaacc gcctaatgga ctacttgcat cgcgcggccg 13440 ccgtgaaccc cgagtatttc accaatgcca tcttgaaccc gcactggcta ccgccccctg 13500 gtttctacac cgggggattc gaggtgcccg agggtaacga tggattcctc tgggacgaca 13560 tagacgacag cgtgttttcc ccgcaaccgc agaccctgct agagttgcaa cagcgcgagc 13620 aggcagaggc ggcgctgcga aaggaaagct tccgcaggcc aagcagcttg tccgatctag 13680 gcgctgcggc cccgcggtca gatgctagta gcccatttcc aagcttgata gggtctctta 13740 ccagcactcg caccacccgc ccgcgcctgc tgggcgagga ggagtaccta aacaactcgc 13800 tgctgcagcc gcagcgcgaa aaaaacctgc ctccggcatt tcccaacaac gggatagaga 13860 gcctagtgga caagatgagt agatggaaga cgtacgcgca ggagcacagg gacgtgccag 13920 gcccgcgccc gcccacccgt cgtcaaaggc acgaccgtca gcggggtctg gtgtgggagg 13980 acgatgactc ggcagacgac agcagcgtcc tggatttggg agggagtggc aacccgtttg 14040 cgcaccttcg ccccaggctg gggagaatgt tttaaaaaaa aaaaagcatg atgcaaaata 14100 aaaaactcac caaggccatg gcaccgagcg ttggttttct tgtattcccc ttagtatgcg 14160 gcgcgcggcg atgtatgagg aaggtcctcc tccctcctac gagagtgtgg tgagcgcggc 14220 gccagtggcg gcggcgctgg gttctccctt cgatgctccc ctggacccgc cgtttgtgcc 14280 tccgcggtac ctgcggccta ccggggggag aaacagcatc cgttactctg agttggcacc 14340 cctattcgac accacccgtg tgtacctggt ggacaacaag tcaacggatg tggcatccct 14400 gaactaccag aacgaccaca gcaactttct gaccacggtc attcaaaaca atgactacag 14460 cccgggggag gcaagcacac agaccatcaa tcttgacgac cggtcgcact ggggcggcga 14520 cctgaaaacc atcctgcata ccaacatgcc aaatgtgaac gagttcatgt ttaccaataa 14580 gtttaaggcg cgggtgatgg tgtcgcgctt gcctactaag gacaatcagg tggagctgaa 14640 atacgagtgg gtggagttca cgctgcccga gggcaactac tccgagacca tgaccataga 14700 ccttatgaac aacgcgatcg tggagcacta cttgaaagtg ggcagacaga acggggttct 14760 ggaaagcgac atcggggtaa agtttgacac ccgcaacttc agactggggt ttgaccccgt 14820 cactggtctt gtcatgcctg gggtatatac aaacgaagcc ttccatccag acatcatttt 14880 gctgccagga tgcggggtgg acttcaccca cagccgcctg agcaacttgt tgggcatccg 14940 caagcggcaa cccttccagg agggctttag gatcacctac gatgatctgg agggtggtaa 15000 cattcccgca ctgttggatg tggacgccta ccaggcgagc ttgaaagatg acaccgaaca 15060 gggcgggggt ggcgcaggcg gcagcaacag cagtggcagc ggcgcggaag agaactccaa 15120 cgcggcagcc gcggcaatgc agccggtgga ggacatgaac gatcatgcca ttcgcggcga 15180 cacctttgcc acacgggctg aggagaagcg cgctgaggcc gaagcagcgg ccgaagctgc 15240 cgcccccgct gcgcaacccg aggtcgagaa gcctcagaag aaaccggtga tcaaacccct 15300 gacagaggac agcaagaaac gcagttacaa cctaataagc aatgacagca ccttcaccca 15360 gtaccgcagc tggtaccttg catacaacta cggcgaccct cagaccggaa tccgctcatg 15420 gaccctgctt tgcactcctg acgtaacctg cggctcggag caggtctact ggtcgttgcc 15480 agacatgatg caagaccccg tgaccttccg ctccacgcgc cagatcagca actttccggt 15540 ggtgggcgcc gagctgttgc ccgtgcactc caagagcttc tacaacgacc aggccgtcta 15600 ctcccaactc atccgccagt ttacctctct gacccacgtg ttcaatcgct ttcccgagaa 15660 ccagattttg gcgcgcccgc cagcccccac catcaccacc gtcagtgaaa acgttcctgc 15720 tctcacagat cacgggacgc taccgctgcg caacagcatc ggaggagtcc agcgagtgac 15780 cattactgac gccagacgcc gcacctgccc ctacgtttac aaggccctgg gcatagtctc 15840 gccgcgcgtc ctatcgagcc gcactttttg agcaagcatg tccatcctta tatcgcccag 15900 caataacaca ggctggggcc tgcgcttccc aagcaagatg tttggcgggg ccaagaagcg 15960 ctccgaccaa cacccagtgc gcgtgcgcgg gcactaccgc gcgccctggg gcgcgcacaa 16020 acgcggccgc actgggcgca ccaccgtcga tgacgccatc gacgcggtgg tggaggaggc 16080 gcgcaactac acgcccacgc cgccaccagt gtccacagtg gacgcggcca ttcagaccgt 16140 ggtgcgcgga gcccggcgct atgctaaaat gaagagacgg cggaggcgcg tagcacgtcg 16200 ccaccgccgc cgacccggca ctgccgccca acgcgcggcg gcggccctgc ttaaccgcgc 16260 acgtcgcacc ggccgacggg cggccatgcg ggccgctcga aggctggccg cgggtattgt 16320 cactgtgccc cccaggtcca ggcgacgagc ggccgccgca gcagccgcgg ccattagtgc 16380 tatgactcag ggtcgcaggg gcaacgtgta ttgggtgcgc gactcggtta gcggcctgcg 16440 cgtgcccgtg cgcacccgcc ccccgcgcaa ctagattgca agaaaaaact acttagactc 16500 gtactgttgt atgtatccag cggcggcggc gcgcaacgaa gctatgtcca agcgcaaaat 16560 caaagaagag atgctccagg tcatcgcgcc ggagatctat ggccccccga agaaggaaga 16620 gcaggattac aagccccgaa agctaaagcg ggtcaaaaag aaaaagaaag atgatgatga 16680 tgaacttgac gacgaggtgg aactgctgca cgctaccgcg cccaggcgac gggtacagtg 16740 gaaaggtcga cgcgtaaaac gtgttttgcg acccggcacc accgtagtct ttacgcccgg 16800 tgagcgctcc acccgcacct acaagcgcgt gtatgatgag gtgtacggcg acgaggacct 16860 gcttgagcag gccaacgagc gcctcgggga gtttgcctac ggaaagcggc ataaggacat 16920 gctggcgttg ccgctggacg agggcaaccc aacacctagc ctaaagcccg taacactgca 16980 gcaggtgctg cccgcgcttg caccgtccga agaaaagcgc ggcctaaagc gcgagtctgg 17040 tgacttggca cccaccgtgc agctgatggt acccaagcgc cagcgactgg aagatgtctt 17100 ggaaaaaatg accgtggaac ctgggctgga gcccgaggtc cgcgtgcggc caatcaagca 17160 ggtggcgccg ggactgggcg tgcagaccgt ggacgttcag atacccacta ccagtagcac 17220 cagtattgcc accgccacag agggcatgga gacacaaacg tccccggttg cctcagcggt 17280 ggcggatgcc gcggtgcagg cggtcgctgc ggccgcgtcc aagacctcta cggaggtgca 17340 aacggacccg tggatgtttc gcgtttcagc cccccggcgc ccgcgcggtt cgaggaagta 17400 cggcgccgcc agcgcgctac tgcccgaata tgccctacat ccttccattg cgcctacccc 17460 cggctatcgt ggctacacct accgccccag aagacgagca actacccgac gccgaaccac 17520 cactggaacc cgccgccgcc gtcgccgtcg ccagcccgtg ctggccccga tttccgtgcg 17580 cagggtggct cgcgaaggag gcaggaccct ggtgctgcca acagcgcgct accaccccag 17640 catcgtttaa aagccggtct ttgtggttct tgcagatatg gccctcacct gccgcctccg 17700 tttcccggtg ccgggattcc gaggaagaat gcaccgtagg aggggcatgg ccggccacgg 17760 cctgacgggc ggcatgcgtc gtgcgcacca ccggcggcgg cgcgcgtcgc accgtcgcat 17820 gcgcggcggt atcctgcccc tccttattcc actgatcgcc gcggcgattg gcgccgtgcc 17880 cggaattgca tccgtggcct tgcaggcgca gagacactga ttaaaaacaa gttgcatgtg 17940 gaaaaatcaa aataaaaagt ctggactctc acgctcgctt ggtcctgtaa ctattttgta 18000 gaatggaaga catcaacttt gcgtctctgg ccccgcgaca cggctcgcgc ccgttcatgg 18060 gaaactggca agatatcggc accagcaata tgagcggtgg cgccttcagc tggggctcgc 18120 tgtggagcgg cattaaaaat ttcggttcca ccgttaagaa ctatggcagc aaggcctgga 18180 acagcagcac aggccagatg ctgagggata agttgaaaga gcaaaatttc caacaaaagg 18240 tggtagatgg cctggcctct ggcattagcg gggtggtgga cctggccaac caggcagtgc 18300 aaaataagat taacagtaag cttgatcccc gccctcccgt agaggagcct ccaccggccg 18360 tggagacagt gtctccagag gggcgtggcg aaaagcgtcc gcgccccgac agggaagaaa 18420 ctctggtgac gcaaatagac gagcctccct cgtacgagga ggcactaaag caaggcctgc 18480 ccaccacccg tcccatcgcg cccatggcta ccggagtgct gggccagcac acacccgtaa 18540 cgctggacct gcctcccccc gccgacaccc agcagaaacc tgtgctgcca ggcccgaccg 18600 ccgttgttgt aacccgtcct agccgcgcgt ccctgcgccg cgccgccagc ggtccgcgat 18660 cgttgcggcc cgtagccagt ggcaactggc aaagcacact gaacagcatc gtgggtctgg 18720 gggtgcaatc cctgaagcgc cgacgatgct tctgaatagc taacgtgtcg tatgtgtgtc 18780 atgtatgcgt ccatgtcgcc gccagaggag ctgctgagcc gccgcgcgcc cgctttccaa 18840 gatggctacc ccttcgatga tgccgcagtg gtcttacatg cacatctcgg gccaggacgc 18900 ctcggagtac ctgagccccg ggctggtgca gtttgcccgc gccaccgaga cgtacttcag 18960 cctgaataac aagtttagaa accccacggt ggcgcctacg cacgacgtga ccacagaccg 19020 gtcccagcgt ttgacgctgc ggttcatccc tgtggaccgt gaggatactg cgtactcgta 19080 caaggcgcgg ttcaccctag ctgtgggtga taaccgtgtg ctggacatgg cttccacgta 19140 ctttgacatc cgcggcgtgc tggacagggg ccctactttt aagccctact ctggcactgc 19200 ctacaacgcc ctggctccca agggtgcccc aaatccttgc gaatgggatg aagctgctac 19260 tgctcttgaa ataaacctag aagaagagga cgatgacaac gaagacgaag tagacgagca 19320 agctgagcag caaaaaactc acgtatttgg gcaggcgcct tattctggta taaatattac 19380 aaaggagggt attcaaatag gtgtcgaagg tcaaacacct aaatatgccg ataaaacatt 19440 tcaacctgaa cctcaaatag gagaatctca gtggtacgaa actgaaatta atcatgcagc 19500 tgggagagtc cttaaaaaga ctaccccaat gaaaccatgt tacggttcat atgcaaaacc 19560 cacaaatgaa aatggagggc aaggcattct tgtaaagcaa caaaatggaa agctagaaag 19620 tcaagtggaa atgcaatttt tctcaactac tgaggcgacc gcaggcaatg gtgataactt 19680 gactcctaaa gtggtattgt acagtgaaga tgtagatata gaaaccccag acactcatat 19740 ttcttacatg cccactatta aggaaggtaa ctcacgagaa ctaatgggcc aacaatctat 19800 gcccaacagg cctaattaca ttgcttttag ggacaatttt attggtctaa tgtattacaa 19860 cagcacgggt aatatgggtg ttctggcggg ccaagcatcg cagttgaatg ctgttgtaga 19920 tttgcaagac agaaacacag agctttcata ccagcttttg cttgattcca ttggtgatag 19980 aaccaggtac ttttctatgt ggaatcaggc tgttgacagc tatgatccag atgttagaat 20040 tattgaaaat catggaactg aagatgaact tccaaattac tgctttccac tgggaggtgt 20100 gattaataca gagactctta ccaaggtaaa acctaaaaca ggtcaggaaa atggatggga 20160 aaaagatgct acagaatttt cagataaaaa tgaaataaga gttggaaata attttgccat 20220 ggaaatcaat ctaaatgcca acctgtggag aaatttcctg tactccaaca tagcgctgta 20280 tttgcccgac aagctaaagt acagtccttc caacgtaaaa atttctgata acccaaacac 20340 ctacgactac atgaacaagc gagtggtggc tcccgggtta gtggactgct acattaacct 20400 tggagcacgc tggtcccttg actatatgga caacgtcaac ccatttaacc accaccgcaa 20460 tgctggcctg cgctaccgct caatgttgct gggcaatggt cgctatgtgc ccttccacat 20520 ccaggtgcct cagaagttct ttgccattaa aaacctcctt ctcctgccgg gctcatacac 20580 ctacgagtgg aacttcagga aggatgttaa catggttctg cagagctccc taggaaatga 20640 cctaagggtt gacggagcca gcattaagtt tgatagcatt tgcctttacg ccaccttctt 20700 ccccatggcc cacaacaccg cctccacgct tgaggccatg cttagaaacg acaccaacga 20760 ccagtccttt aacgactatc tctccgccgc caacatgctc taccctatac ccgccaacgc 20820 taccaacgtg cccatatcca tcccctcccg caactgggcg gctttccgcg gctgggcctt 20880 cacgcgcctt aagactaagg aaaccccatc actgggctcg ggctacgacc cttattacac 20940 ctactctggc tctataccct acctagatgg aaccttttac ctcaaccaca cctttaagaa 21000 ggtggccatt acctttgact cttctgtcag ctggcctggc aatgaccgcc tgcttacccc 21060 caacgagttt gaaattaagc gctcagttga cggggagggt tacaacgttg cccagtgtaa 21120 catgaccaaa gactggttcc tggtacaaat gctagctaac tacaacattg gctaccaggg 21180 cttctatatc ccagagagct acaaggaccg catgtactcc ttctttagaa acttccagcc 21240 catgagccgt caggtggtgg atgatactaa atacaaggac taccaacagg tgggcatcct 21300 acaccaacac aacaactctg gatttgttgg ctaccttgcc cccaccatgc gcgaaggaca 21360 ggcctaccct gctaacttcc cctatccgct tataggcaag accgcagttg acagcattac 21420 ccagaaaaag tttctttgcg atcgcaccct ttggcgcatc ccattctcca gtaactttat 21480 gtccatgggc gcactcacag acctgggcca aaaccttctc tacgccaact ccgcccacgc 21540 gctagacatg acttttgagg tggatcccat ggacgagccc acccttcttt atgttttgtt 21600 tgaagtcttt gacgtggtcc gtgtgcaccg gccgcaccgc ggcgtcatcg aaaccgtgta 21660 cctgcgcacg cccttctcgg ccggcaacgc cacaacataa agaagcaagc aacatcaaca 21720 acagctgccg ccatgggctc cagtgagcag gaactgaaag ccattgtcaa agatcttggt 21780 tgtgggccat attttttggg cacctatgac aagcgctttc caggctttgt ttctccacac 21840 aagctcgcct gcgccatagt caatacggcc ggtcgcgaga ctgggggcgt acactggatg 21900 gcctttgcct ggaacccgca ctcaaaaaca tgctacctct ttgagccctt tggcttttct 21960 gaccagcgac tcaagcaggt ttaccagttt gagtacgagt cactcctgcg ccgtagcgcc 22020 attgcttctt cccccgaccg ctgtataacg ctggaaaagt ccacccaaag cgtacagggg 22080 cccaactcgg ccgcctgtgg actattctgc tgcatgtttc tccacgcctt tgccaactgg 22140 ccccaaactc ccatggatca caaccccacc atgaacctta ttaccggggt acccaactcc 22200 atgctcaaca gtccccaggt acagcccacc ctgcgtcgca accaggaaca gctctacagc 22260 ttcctggagc gccactcgcc ctacttccgc agccacagtg cgcagattag gagcgccact 22320 tctttttgtc acttgaaaaa catgtaaaaa taatgtacta gagacacttt caataaaggc 22380 aaatgctttt atttgtacac tctcgggtga ttatttaccc ccacccttgc cgtctgcgcc 22440 gtttaaaaat caaaggggtt ctgccgcgca tcgctatgcg ccactggcag ggacacgttg 22500 cgatactggt gtttagtgct ccacttaaac tcaggcacaa ccatccgcgg cagctcggtg 22560 aagttttcac tccacaggct gcgcaccatc accaacgcgt ttagcaggtc gggcgccgat 22620 atcttgaagt cgcagttggg gcctccgccc tgcgcgcgcg agttgcgata cacagggttg 22680 cagcactgga acactatcag cgccgggtgg tgcacgctgg ccagcacgct cttgtcggag 22740 atcagatccg cgtccaggtc ctccgcgttg ctcagggcga acggagtcaa ctttggtagc 22800 tgccttccca aaaagggcgc gtgcccaggc tttgagttgc actcgcaccg tagtggcatc 22860 aaaaggtgac cgtgcccggt ctgggcgtta ggatacagcg cctgcataaa agccttgatc 22920 tgcttaaaag ccacctgagc ctttgcgcct tcagagaaga acatgccgca agacttgccg 22980 gaaaactgat tggccggaca ggccgcgtcg tgcacgcagc accttgcgtc ggtgttggag 23040 atctgcacca catttcggcc ccaccggttc ttcacgatct tggccttgct agactgctcc 23100 ttcagcgcgc gctgcccgtt ttcgctcgtc acatccattt caatcacgtg ctccttattt 23160 atcataatgc ttccgtgtag acacttaagc tcgccttcga tctcagcgca gcggtgcagc 23220 cacaacgcgc agcccgtggg ctcgtgatgc ttgtaggtca cctctgcaaa cgactgcagg 23280 tacgcctgca ggaatcgccc catcatcgtc acaaaggtct tgttgctggt gaaggtcagc 23340 tgcaacccgc ggtgctcctc gttcagccag gtcttgcata cggccgccag agcttccact 23400 tggtcaggca gtagtttgaa gttcgccttt agatcgttat ccacgtggta cttgtccatc 23460 agcgcgcgcg cagcctccat gcccttctcc cacgcagaca cgatcggcac actcagcggg 23520 ttcatcaccg taatttcact ttccgcttcg ctgggctctt cctcttcctc ttgcgtccgc 23580 ataccacgcg ccactgggtc gtcttcattc agccgccgca ctgtgcgctt acctcctttg 23640 ccatgcttga ttagcaccgg tgggttgctg aaacccacca tttgtagcgc cacatcttct 23700 ctttcttcct cgctgtccac gattacctct ggtgatggcg ggcgctcggg cttgggagaa 23760 gggcgcttct ttttcttctt gggcgcaatg gccaaatccg ccgccgaggt cgatggccgc 23820 gggctgggtg tgcgcggcac cagcgcgtct tgtgatgagt cttcctcgtc ctcggactcg 23880 atacgccgcc tcatccgctt ttttgggggc gcccggggag gcggcggcga cggggacggg 23940 gacgacacgt cctccatggt tgggggacgt cgcgccgcac cgcgtccgcg ctcgggggtg 24000 gtttcgcgct gctcctcttc ccgactggcc atttccttct cctataggca gaaaaagatc 24060 atggagtcag tcgagaagaa ggacagccta accgccccct ctgagttcgc caccaccgcc 24120 tccaccgatg ccgccaacgc gcctaccacc ttccccgtcg aggcaccccc gcttgaggag 24180 gaggaagtga ttatcgagca ggacccaggt tttgtaagcg aagacgacga ggaccgctca 24240 gtaccaacag aggataaaaa gcaagaccag gacaacgcag aggcaaacga ggaacaagtc 24300 gggcgggggg acgaaaggca tggcgactac ctagatgtgg gagacgacgt gctgttgaag 24360 catctgcagc gccagtgcgc cattatctgc gacgcgttgc aagagcgcag cgatgtgccc 24420 ctcgccatag cggatgtcag ccttgcctac gaacgccacc tattctcacc gcgcgtaccc 24480 cccaaacgcc aagaaaacgg cacatgcgag cccaacccgc gcctcaactt ctaccccgta 24540 tttgccgtgc cagaggtgct tgccacctat cacatctttt tccaaaactg caagataccc 24600 ctatcctgcc gtgccaaccg cagccgagcg gacaagcagc tggccttgcg gcagggcgct 24660 gtcatacctg atatcgcctc gctcaacgaa gtgccaaaaa tctttgaggg tcttggacgc 24720 gacgagaagc gcgcggcaaa cgctctgcaa caggaaaaca gcgaaaatga aagtcactct 24780 ggagtgttgg tggaactcga gggtgacaac gcgcgcctag ccgtactaaa acgcagcatc 24840 gaggtcaccc actttgccta cccggcactt aacctacccc ccaaggtcat gagcacagtc 24900 atgagtgagc tgatcgtgcg ccgtgcgcag cccctggaga gggatgcaaa tttgcaagaa 24960 caaacagagg agggcctacc cgcagttggc gacgagcagc tagcgcgctg gcttcaaacg 25020 cgcgagcctg ccgacttgga ggagcgacgc aaactaatga tggccgcagt gctcgttacc 25080 gtggagcttg agtgcatgca gcggttcttt gctgacccgg agatgcagcg caagctagag 25140 gaaacattgc actacacctt tcgacagggc tacgtacgcc aggcctgcaa gatctccaac 25200 gtggagctct gcaacctggt ctcctacctt ggaattttgc acgaaaaccg ccttgggcaa 25260 aacgtgcttc attccacgct caagggcgag gcgcgccgcg actacgtccg cgactgcgtt 25320 tacttatttc tatgctacac ctggcagacg gccatgggcg tttggcagca gtgcttggag 25380 gagtgcaacc tcaaggagct gcagaaactg ctaaagcaaa acttgaagga cctatggacg 25440 gccttcaacg agcgctccgt ggccgcgcac ctggcggaca tcattttccc cgaacgcctg 25500 cttaaaaccc tgcaacaggg tctgccagac ttcaccagtc aaagcatgtt gcagaacttt 25560 aggaacttta tcctagagcg ctcaggaatc ttgcccgcca cctgctgtgc acttcctagc 25620 gactttgtgc ccattaagta ccgcgaatgc cctccgccgc tttggggcca ctgctacctt 25680 ctgcagctag ccaactacct tgcctaccac tctgacataa tggaagacgt gagcggtgac 25740 ggtctactgg agtgtcactg tcgctgcaac ctatgcaccc cgcaccgctc cctggtttgc 25800 aattcgcagc tgcttaacga aagtcaaatt atcggtacct ttgagctgca gggtccctcg 25860 cctgacgaaa agtccgcggc tccggggttg aaactcactc cggggctgtg gacgtcggct 25920 taccttcgca aatttgtacc tgaggactac cacgcccacg agattaggtt ctacgaagac 25980 caatcccgcc cgccaaatgc ggagcttacc gcctgcgtca ttacccaggg ccacattctt 26040 ggccaattgc aagccatcaa caaagcccgc caagagtttc tgctacgaaa gggacggggg 26100 gtttacttgg acccccagtc cggcgaggag ctcaacccaa tccccccgcc gccgcagccc 26160 tatcagcagc agccgcgggc ccttgcttcc caggatggca cccaaaaaga agctgcagct 26220 gccgccgcca cccacggacg aggaggaata ctgggacagt caggcagagg aggttttgga 26280 cgaggaggag gaggacatga tggaagactg ggagagccta gacgaggaag cttccgaggt 26340 cgaagaggtg tcagacgaaa caccgtcacc ctcggtcgca ttcccctcgc cggcgcccca 26400 gaaatcggca accggttcca gcatggctac aacctccgct cctcaggcgc cgccggcact 26460 gcccgttcgc cgacccaacc gtagatggga caccactgga accagggccg gtaagtccaa 26520 gcagccgccg ccgttagccc aagagcaaca acagcgccaa ggctaccgct catggcgcgg 26580 gcacaagaac gccatagttg cttgcttgca agactgtggg ggcaacatct ccttcgcccg 26640 ccgctttctt ctctaccatc acggcgtggc cttcccccgt aacatcctgc attactaccg 26700 tcatctctac agcccatact gcaccggcgg cagcggcagc ggcagcaaca gcagcggcca 26760 cacagaagca aaggcgaccg gatagcaaga ctctgacaaa gcccaagaaa tccacagcgg 26820 cggcagcagc aggaggagga gcgctgcgtc tggcgcccaa cgaacccgta tcgacccgcg 26880 agcttagaaa caggattttt cccactctgt atgctatatt tcaacagagc aggggccaag 26940 aacaagagct gaaaataaaa aacaggtctc tgcgatccct cacccgcagc tgcctgtatc 27000 acaaaagcga agatcagctt cggcgcacgc tggaagacgc ggaggctctc ttcagtaaat 27060 actgcgcgct gactcttaag gactagtttc gcgccctttc tcaaatttaa gcgcgaaaac 27120 tacgtcatct ccagcggcca cacccggcgc cagcacctgt cgtcagcgcc attatgagca 27180 aggaaattcc cacgccctac atgtggagtt accagccaca aatgggactt gcggctggag 27240 ctgcccaaga ctactcaacc cgaataaact acatgagcgc gggaccccac atgatatccc 27300 gggtcaacgg aatccgcgcc caccgaaacc gaattctctt ggaacaggcg gctattacca 27360 ccacacctcg taataacctt aatccccgta gttggcccgc tgccctggtg taccaggaaa 27420 gtcccgctcc caccactgtg gtacttccca gagacgccca ggccgaagtt cagatgacta 27480 actcaggggc gcagcttgcg ggcggctttc gtcacagggt gcggtcgccc gggcagggta 27540 taactcacct gacaatcaga gggcgaggta ttcagctcaa cgacgagtcg gtgagctcct 27600 cgcttggtct ccgtccggac gggacatttc agatcggcgg cgccggccgt ccttcattca 27660 cgcctcgtca ggcaatccta actctgcaga cctcgtcctc tgagccgcgc tctggaggca 27720 ttggaactct gcaatttatt gaggagtttg tgccatcggt ctactttaac cccttctcgg 27780 gacctcccgg ccactatccg gatcaattta ttcctaactt tgacgcggta aaggactcgg 27840 cggacggcta cgactgaatg ttaagtggag aggcagagca actgcgcctg aaacacctgg 27900 tccactgtcg ccgccacaag tgctttgccc gcgactccgg tgagttttgc tactttgaat 27960 tgcccgagga tcatatcgag ggcccggcgc acggcgtccg gcttaccgcc cagggagagc 28020 ttgcccgtag cctgattcgg gagtttaccc agcgccccct gctagttgag cgggacaggg 28080 gaccctgtgt tctcactgtg atttgcaact gtcctaacct tggattacat caagatcttt 28140 gttgccatct ctgtgctgag tataataaat acagaaatta aaatatactg gggctcctat 28200 cgccatcctg taaacgccac cgtcttcacc cgcccaagca aaccaaggcg aaccttacct 28260 ggtactttta acatctctcc ctctgtgatt tacaacagtt tcaacccaga cggagtgagt 28320 ctacgagaga acctctccga gctcagctac tccatcagaa aaaacaccac cctccttacc 28380 tgccgggaac gtacgagtgc gtcaccggcc gctgcaccac acctaccgcc tgaccgtaaa 28440 ccagactttt tccggacaga cctcaataac tctgtttacc agaacaggag gtgagcttag 28500 aaaaccctta gggtattagg ccaaaggcgc agctactgtg gggtttatga acaattcaag 28560 caactctacg ggctattcta attcaggttt ctctagaatc ggggttgggg ttattctctg 28620 tcttgtgatt ctctttattc ttatactaac gcttctctgc ctaaggctcg ccgcctgctg 28680 tgtgcacatt tgcatttatt gtcagctttt taaacgctgg ggtcgccacc caagatgatt 28740 aggtacataa tcctaggttt actcaccctt gcgtcagccc acggtaccac ccaaaaggtg 28800 gattttaagg agccagcctg taatgttaca ttcgcagctg aagctaatga gtgcaccact 28860 cttataaaat gcaccacaga acatgaaaag ctgcttattc gccacaaaaa caaaattggc 28920 aagtatgctg tttatgctat ttggcagcca ggtgacacta cagagtataa tgttacagtt 28980 ttccagggta aaagtcataa aacttttatg tatacttttc cattttatga aatgtgcgac 29040 attaccatgt acatgagcaa acagtataag ttgtggcccc cacaaaattg tgtggaaaac 29100 actggcactt tctgctgcac tgctatgcta attacagtgc tcgctttggt ctgtacccta 29160 ctctatatta aatacaaaag cagacgcagc tttattgagg aaaagaaaat gccttaattt 29220 actaagttac aaagctaatg tcaccactaa ctgctttact cgctgcttgc aaaacaaatt 29280 caaaaagtta gcattataat tagaatagga tttaaacccc ccggtcattt cctgctcaat 29340 accattcccc tgaacaattg actctatgtg ggatatgctc cagcgctaca accttgaagt 29400 caggcttcct ggatgtcagc atctgacttt ggccagcacc tgtcccgcgg atttgttcca 29460 gtccaactac agcgacccac cctaacagag atgaccaaca caaccaacgc ggccgccgct 29520 accggactta catctaccac aaatacaccc caagtttctg cctttgtcaa taactgggat 29580 aacttgggca tgtggtggtt ctccatagcg cttatgtttg tatgccttat tattatgtgg 29640 ctcatctgct gcctaaagcg caaacgcgcc cgaccaccca tctatagtcc catcattgtg 29700 ctacacccaa acaatgatgg aatccataga ttggacggac tgaaacacat gttcttttct 29760 cttacagtat gattaaatga gacatgattc ctcgagtttt tatattactg acccttgttg 29820 cgcttttttg tgcgtgctcc acattggctg cggtttctca catcgaagta gactgcattc 29880 cagccttcac agtctatttg ctttacggat ttgtcaccct cacgctcatc tgcagcctca 29940 tcactgtggt catcgccttt atccagtgca ttgactgggt ctgtgtgcgc tttgcatatc 30000 tcagacacca tccccagtac agggacagga ctatagctga gcttcttaga attctttaat 30060 tatgaaattt actgtgactt ttctgctgat tatttgcacc ctatctgcgt tttgttcccc 30120 gacctccaag cctcaaagac atatatcatg cagattcact cgtatatgga atattccaag 30180 ttgctacaat gaaaaaagcg atctttccga agcctggtta tatgcaatca tctctgttat 30240 ggtgttctgc agtaccatct tagccctagc tatatatccc taccttgaca ttggctggaa 30300 acgaatagat gccatgaacc acccaacttt ccccgcgccc gctatgcttc cactgcaaca 30360 agttgttgcc ggcggctttg tcccagccaa tcagcctcgc cccacttctc ccacccccac 30420 tgaaatcagc tactttaatc taacaggagg agatgactga caccctagat ctagaaatgg 30480 acggaattat tacagagcag cgcctgctag aaagacgcag ggcagcggcc gagcaacagc 30540 gcatgaatca agagctccaa gacatggtta acttgcacca gtgcaaaagg ggtatctttt 30600 gtctggtaaa gcaggccaaa gtcacctacg acagtaatac caccggacac cgccttagct 30660 acaagttgcc aaccaagcgt cagaaattgg tggtcatggt gggagaaaag cccattacca 30720 taactcagca ctcggtagaa accgaaggct gcattcactc accttgtcaa ggacctgagg 30780 atctctgcac ccttattaag accctgtgcg gtctcaaaga tcttattccc tttaactaat 30840 aaaaaaaaat aataaagcat cacttactta aaatcagtta gcaaatttct gtccagttta 30900 ttcagcagca cctccttgcc ctcctcccag ctctggtatt gcagcttcct cctggctgca 30960 aactttctcc acaatctaaa tggaatgtca gtttcctcct gttcctgtcc atccgcaccc 31020 actatcttca tgttgttgca gatgaagcgc gcaagaccgt ctgaagatac cttcaacccc 31080 gtgtatccat atgacacgga aaccggtcct ccaactgtgc cttttcttac tcctcccttt 31140 gtatccccca atgggtttca agagagtccc cctggggtac tctctttgcg cctatccgaa 31200 cctctagtta cctccaatgg catgcttgcg ctcaaaatgg gcaacggcct ctctctggac 31260 gaggccggca accttacctc ccaaaatgta accactgtga gcccacctct caaaaaaacc 31320 aagtcaaaca taaacctgga aatatctgca cccctcacag ttacctcaga agccctaact 31380 gtggctgccg ccgcacctct aatggtcgcg ggcaacacac tcaccatgca atcacaggcc 31440 ccgctaaccg tgcacgactc caaacttagc attgccaccc aaggacccct cacagtgtca 31500 gaaggaaagc tagccctgca aacatcaggc cccctcacca ccaccgatag cagtaccctt 31560 actatcactg cctcaccccc tctaactact gccactggta gcttgggcat tgacttgaaa 31620 gagcccattt atacacaaaa tggaaaacta ggactaaagt acggggctcc tttgcatgta 31680 acagacgacc taaacacttt gaccgtagca actggtccag gtgtgactat taataatact 31740 tccttgcaaa ctaaagttac tggagccttg ggttttgatt cacaaggcaa tatgcaactt 31800 aatgtagcag gaggactaag gattgattct caaaacagac gccttatact tgatgttagt 31860 tatccgtttg atgctcaaaa ccaactaaat ctaagactag gacagggccc tctttttata 31920 aactcagccc acaacttgga tattaactac aacaaaggcc tttacttgtt tacagcttca 31980 aacaattcca aaaagcttga ggttaaccta agcactgcca aggggttgat gtttgacgct 32040 acagccatag ccattaatgc aggagatggg cttgaatttg gttcacctaa tgcaccaaac 32100 acaaatcccc tcaaaacaaa aattggccat ggcctagaat ttgattcaaa caaggctatg 32160 gttcctaaac taggaactgg ccttagtttt gacagcacag gtgccattac agtaggaaac 32220 aaaaataatg ataagctaac tttgtggacc acaccagctc catctcctaa ctgtagacta 32280 aatgcagaga aagatgctaa actcactttg gtcttaacaa aatgtggcag tcaaatactt 32340 gctacagttt cagttttggc tgttaaaggc agtttggctc caatatctgg aacagttcaa 32400 agtgctcatc ttattataag atttgacgaa aatggagtgc tactaaacaa ttccttcctg 32460 gacccagaat attggaactt tagaaatgga gatcttactg aaggcacagc ctatacaaac 32520 gctgttggat ttatgcctaa cctatcagct tatccaaaat ctcacggtaa aactgccaaa 32580 agtaacattg tcagtcaagt ttacttaaac ggagacaaaa ctaaacctgt aacactaacc 32640 attacactaa acggtacaca ggaaacagga gacacaactc caagtgcata ctctatgtca 32700 ttttcatggg actggtctgg ccacaactac attaatgaaa tatttgccac atcctcttac 32760 actttttcat acattgccca agaataaaga atcgtttgtg ttatgtttca acgtgtttat 32820 ttttcaattg cagaaaattt caagtcattt ttcattcagt agtatagccc caccaccaca 32880 tagcttatac agatcaccgt accttaatca aactcacaga accctagtat tcaacctgcc 32940 acctccctcc caacacacag agtacacagt cctttctccc cggctggcct taaaaagcat 33000 catatcatgg gtaacagaca tattcttagg tgttatattc cacacggttt cctgtcgagc 33060 caaacgctca tcagtgatat taataaactc cccgggcagc tcacttaagt tcatgtcgct 33120 gtccagctgc tgagccacag gctgctgtcc aacttgcggt tgcttaacgg gcggcgaagg 33180 agaagtccac gcctacatgg gggtagagtc ataatcgtgc atcaggatag ggcggtggtg 33240 ctgcagcagc gcgcgaataa actgctgccg ccgccgctcc gtcctgcagg aatacaacat 33300 ggcagtggtc tcctcagcga tgattcgcac cgcccgcagc ataaggcgcc ttgtcctccg 33360 ggcacagcag cgcaccctga tctcacttaa atcagcacag taactgcagc acagcaccac 33420 aatattgttc aaaatcccac agtgcaaggc gctgtatcca aagctcatgg cggggaccac 33480 agaacccacg tggccatcat accacaagcg caggtagatt aagtggcgac ccctcataaa 33540 cacgctggac ataaacatta cctcttttgg catgttgtaa ttcaccacct cccggtacca 33600 tataaacctc tgattaaaca tggcgccatc caccaccatc ctaaaccagc tggccaaaac 33660 ctgcccgccg gctatacact gcagggaacc gggactggaa caatgacagt ggagagccca 33720 ggactcgtaa ccatggatca tcatgctcgt catgatatca atgttggcac aacacaggca 33780 cacgtgcata cacttcctca ggattacaag ctcctcccgc gttagaacca tatcccaggg 33840 aacaacccat tcctgaatca gcgtaaatcc cacactgcag ggaagacctc gcacgtaact 33900 cacgttgtgc attgtcaaag tgttacattc gggcagcagc ggatgatcct ccagtatggt 33960 agcgcgggtt tctgtctcaa aaggaggtag acgatcccta ctgtacggag tgcgccgaga 34020 caaccgagat cgtgttggtc gtagtgtcat gccaaatgga acgccggacg tagtcatatt 34080 tcctgaagca aaaccaggtg cgggcgtgac aaacagatct gcgtctccgg tctcgccgct 34140 tagatcgctc tgtgtagtag ttgtagtata tccactctct caaagcatcc aggcgccccc 34200 tggcttcggg ttctatgtaa actccttcat gcgccgctgc cctgataaca tccaccaccg 34260 cagaataagc cacacccagc caacctacac attcgttctg cgagtcacac acgggaggag 34320 cgggaagagc tggaagaacc atgttttttt ttttattcca aaagattatc caaaacctca 34380 aaatgaagat ctattaagtg aacgcgctcc cctccggtgg cgtggtcaaa ctctacagcc 34440 aaagaacaga taatggcatt tgtaagatgt tgcacaatgg cttccaaaag gcaaacggcc 34500 ctcacgtcca agtggacgta aaggctaaac ccttcagggt gaatctcctc tataaacatt 34560 ccagcacctt caaccatgcc caaataattc tcatctcgcc accttctcaa tatatctcta 34620 agcaaatccc gaatattaag tccggccatt gtaaaaatct gctccagagc gccctccacc 34680 ttcagcctca agcagcgaat catgattgca aaaattcagg ttcctcacag acctgtataa 34740 gattcaaaag cggaacatta acaaaaatac cgcgatcccg taggtccctt cgcagggcca 34800 gctgaacata atcgtgcagg tctgcacgga ccagcgcggc cacttccccg ccaggaacct 34860 tgacaaaaga acccacactg attatgacac gcatactcgg agctatgcta accagcgtag 34920 ccccgatgta agctttgttg catgggcggc gatataaaat gcaaggtgct gctcaaaaaa 34980 tcaggcaaag cctcgcgcaa aaaagaaagc acatcgtagt catgctcatg cagataaagg 35040 caggtaagct ccggaaccac cacagaaaaa gacaccattt ttctctcaaa catgtctgcg 35100 ggtttctgca taaacacaaa ataaaataac aaaaaaacat ttaaacatta gaagcctgtc 35160 ttacaacagg aaaaacaacc cttataagca taagacggac tacggccatg ccggcgtgac 35220 cgtaaaaaaa ctggtcaccg tgattaaaaa gcaccaccga cagctcctcg gtcatgtccg 35280 gagtcataat gtaagactcg gtaaacacat caggttgatt catcggtcag tgctaaaaag 35340 cgaccgaaat agcccggggg aatacatacc cgcaggcgta gagacaacat tacagccccc 35400 ataggaggta taacaaaatt aataggagag aaaaacacat aaacacctga aaaaccctcc 35460 tgcctaggca aaatagcacc ctcccgctcc agaacaacat acagcgcttc acagcggcag 35520 cctaacagtc agccttacca gtaaaaaaga aaacctatta aaaaaacacc actcgacacg 35580 gcaccagctc aatcagtcac agtgtaaaaa agggccaagt gcagagcgag tatatatagg 35640 actaaaaaat gacgtaacgg ttaaagtcca caaaaaacac ccagaaaacc gcacgcgaac 35700 ctacgcccag aaacgaaagc caaaaaaccc acaacttcct caaatcgtca cttccgtttt 35760 cccacgttac gtaacttccc attttaagaa aactacaatt cccaacacat acaagttact 35820 ccgccctaaa acctacgtca cccgccccgt tcccacgccc cgcgccacgt cacaaactcc 35880 accccctcat tatcatattg gcttcaatcc aaaataaggt atattattga tgatg 35935 5 16 DNA Artificial Sequence This is a PCR primer 5 ctatcctgag acggac 16 6 34 DNA artificial sequence This is a PCR primer 6 gatcggatcc aggtctccag taagtggtag ctgc 34 7 25 DNA artificial sequence This is a PCR primer 7 aaaggataaa tggagtaaag aaacc 25 8 23 DNA artificial sequence This is a PCR primer 8 cagatgggtt tgttcattta tcc 23 

What is claimed is:
 1. A method for ablating tumor cells in a subject having at least one tumor site, the method comprising: (a) contacting the tumor cells in at least one tumor with a lytic agent in vivo, under lytic conditions, forming a treated tumor; and (b) applying a sufficient in vivo stimulus to the treated tumor forming a stimulated tumor.
 2. The method of claim 1, wherein contacting the tumor cells with a lytic agent occurs before applying the in vivo stimulus; or applying the in vivo stimulus to the tumor occurs before contacting the tumor cells with a lytic agent; or contacting the tumor cells with a lytic agent and the applying the in vivo stimulus occur simultaneously.
 3. The method of claim 1, further comprising: waiting a first period of time after contacting the tumor cells in at least one tumor with a lytic agent in vivo, but before applying the in vivo stimulus.
 4. The method of claim 3, further comprising: repeating following method steps for a first-number of rounds: (a) contacting the tumor cells in the treated tumor with the lytic agent in vivo; waiting a period of time; and (b) applying an in vivo stimulus to the treated tumor.
 5. The method of claim 4, wherein the first-number of rounds is in a range of 1 to about 5 rounds.
 6. The method of claim 4, wherein the first period of time is about 1 to about 10 days.
 7. The method of claim 4, further comprising: applying an in vivo stimulus to the treated tumor for a second-number of rounds:
 8. The method of claim 7, wherein the second-number of rounds is in a range of about 1 to about 16 rounds.
 9. The method of claim 1, wherein applying the stimulus is for about 15 minutes to about 90 minutes.
 10. The method of claim 1, wherein the tumor comprises: a nasopharyngeal carcinoma, a chondrosarcoma, a cancer of the colon, Dukes's D, and non-small cell lung cancer.
 11. The method of claim 1, wherein the tumor cells are cells of breast cancer, prostate cancer, ovarian cancer, malignant hepatoma, carcinoma of esophagus, small cell lung cancer, lung cancer, cancer of rectum, carcinoma of stomach, carcinoma of ovarium, ascites, or melanoma.
 12. The method of claim 1, wherein the lytic agent comprises an isolated oncolytic virus that replicates in the tumor cells and is inhibited from replicating in non-tumor cells; and wherein the lytic conditions comprise infective conditions.
 13. The method of claim 12, wherein the isolated oncolytic virus comprises an adenovirus not having a functional viral oncoprotein; and wherein tumor cells lack a functional p53-or a functional RB-gene product.
 14. The method of claim 13, wherein the functional viral oncoprotein comprises a p53- or RB-binding protein.
 15. The method of claim 1, wherein the lytic agent comprises an isolated oncolytic virus having a sequence at least 95% identical to SeqID#1 or a sequence at least 95% identical to SeqID#2; and the lytic conditions comprise infective conditions.
 16. The method of claim 1, wherein the isolated oncolytic virus is an isolated herpes simplex virus, an isolated reovirus, an isolated newcastle virus, an isolated poliovirus, an isolated measles virus, or an isolated vesicular stomatis virus.
 17. The method of claim 1, wherein the lytic agent comprises an oncolytic bacteria.
 18. The method of claim 17, wherein the oncolytic bacteria is Salmonella, Bifidobacterium, Shigella, Listeria, Yersinia or Clostridium.
 19. The method of claim 1, wherein the lytic agent comprises an isolated nucleic acid expression construct that encodes a gene comprising: an apoptotic gene, a cytolytic gene, a tumor necrosis factor gene, a negative I-κ-β gene, a caspase gene, a γ-globulin gene, or a hα-1 antitrypsin, wherein the encoded gene is used for the purpose of oncolysis.
 20. The method of claim 1, wherein the in vivo stimulus comprises a local hyperthermia in a range of about 1 to about 7 degrees Celsius above a normal body temperature for the subject.
 21. The method of claim 1, wherein the in vivo stimulus comprises high-frequency electromagnetic pulses.
 22. The method of claim 1, wherein the in vivo stimulus comprises radiofrequency diathermy, wherein the radiofrequency is in the range of 0.1 to 100 MHz.
 23. The method of claim 1, wherein the in vivo stimulus comprises microwave diathermy, wherein the microwave is in the range of 100 to 2,450 MHz.
 24. The method of claim 1, wherein the stimulus comprises a ultrasound diathermy.
 25. The method of claim 1, wherein the an in vivo stimulus comprises a systemic hyperthermia.
 26. The method of claim 1, wherein the stimulus is an anoxia, a radiation, an alcohol, or a glutamine treatment, or infection.
 27. The method of claim 1, wherein, the stimulated tumor expresses at least one chaperone protein at an elevated level compared to that of the tumor prior to applying the stimulus and wherein the chaperone protein comprises a heat shock protein (“HSP”).
 28. The method of claim 27, wherein the heat shock protein is HSP 70, Hsp30, Hsp60, Hsp90, Hsp94, Hsp96, or Hsp
 110. 29. A method for ablating tumor cells in a subject having at least a first tumor and a distal tumor, the method comprising: (a) contacting the tumor cells in the first-tumor with a lytic agent in vivo, under lytic conditions, forming a treated first-tumor, the distal tumor is not contacted with the lytic agent; and (b) applying an in vivo stimulus to the treated first-tumor forming a stimulated first-tumor, the distal tumor is not stimulated.
 30. The method of claim 29, wherein contacting the tumor cells of the first tumor with a lytic agent occurs before applying the in vivo stimulus; or applying the in vivo stimulus to the tumor occurs before contacting the tumor cells with a lytic agent; or contacting the tumor cells with a lytic agent and the applying the in vivo stimulus occur simultaneously.
 31. The method of claim 29, further comprising: waiting a first period of time after contacting the tumor cells in at least one tumor with a lytic agent in vivo, but before applying the in vivo stimulus.
 32. The method of claim 31, further comprising: repeating following method steps for a first-number of rounds: (a) contacting the tumor cells in the first-tumor with the lytic agent in vivo; waiting a period of time; and (b) applying the in vivo stimulus to the treated first-tumor.
 33. The method of claim 32, wherein the first-number of rounds is in a range of 1 to about 5 rounds.
 34. The method of claim 32, wherein the first period of time is about 1 to about 10 days.
 35. The method of claim 32, further comprising: repeating applying an in vivo stimulus to the treated first-tumor for a second-number of rounds:
 36. The method of claim 32, wherein the second-number of rounds is in a range of about 1 to about 16 rounds.
 37. The method of claim 29, wherein applying the stimulus is for about 15 minutes to about 90 minutes.
 38. The method of claim 29, wherein the first tumor is a nasopharyngeal carcinoma, a chondrosarcoma, a cancer of the colon, Dukes's D, or a non-small cell lung cancer and the distal-tumor comprises a metastasis thereof.
 39. The method of claim 29, wherein the tumor cells of the first tumor are cells of breast cancer, prostate cancer, ovarian cancer, malignant hepatoma, carcinoma of esophagus, small cell lung cancer, lung cancer, cancer of rectum, carcinoma of stomach, carcinoma of ovarium, ascites or melanoma; and the distal-tumor comprises a metastasis thereof.
 40. The method of claim 29, wherein the lytic agent comprises an isolated oncolytic virus that replicates in the tumor cells and is inhibited from replicating in non-tumor cells; and wherein the lytic conditions comprise infective conditions.
 41. The method of claim 40, wherein the isolated oncolytic virus comprises an adenovirus not having a functional viral oncoprotein; and wherein tumor cells lack a functional p53- or a functional RB-gene product.
 42. The method of claim 41, wherein the functional viral oncoprotein comprises a p53- or RB-binding protein.
 43. The method of claim 29, wherein the lytic agent comprises an isolated oncolytic virus having a sequence at least 95% identical to SeqID#1 or a sequence at least 95% identical to SeqID#2; and the lytic conditions comprise infective conditions.
 44. The method of claim 29, wherein the isolated oncolytic virus is an isolated herpes simplex virus, an isolated reovirus, an isolated newcastle virus, an isolated poliovirus, an isolated measles virus, or an isolated vesicular stomatis virus.
 45. The method of claim 29, wherein the lytic agent comprises an oncolytic bacteria.
 46. The method of claim 45, wherein the oncolytic bacteria is Salmonella, Bifidobacterium, Shigella, Listeria, Yersinia or Clostridium.
 47. The method of claim 29, wherein the lytic agent comprises an isolated nucleic acid expression construct that encodes a gene comprising: an apoptotic gene, a cytolytic gene, a tumor necrosis factor gene, a negative I-κ-β gene, a caspase gene, a γ-globulin gene, or a hα-1 antitrypsin, wherein the encoded gene is used for the purpose of oncolysis.
 48. The method of claim 29, wherein the in vivo stimulus comprises a local hyperthermia in a range of about 1 to about 7 degrees Celsius above a normal body temperature for the subject.
 49. The method of claim 29, wherein the in vivo stimulus comprises high-frequency electromagnetic pulses.
 50. The method of claim 29, wherein the in vivo stimulus comprises radiofrequency diathermy, wherein the radiofrequency is in the range of 0.1 to 100 MHz.
 51. The method of claim 29, wherein the in vivo stimulus comprises microwave diathermy, wherein the microwave is in the range of 100 to 2,450 MHz.
 52. The method of claim 29, wherein the stimulus comprises a ultrasound diathermy.
 53. The method of claim 29, wherein the an in vivo stimulus comprises a systemic hyperthermia.
 54. The method of claim 29, wherein the stimulus is an anoxia, a radiation, an alcohol, or a glutamine treatment, or infection.
 55. The method of claim 29, wherein, the stimulated first tumor expresses at least one chaperone protein at an elevated level compared to that of the tumor prior to applying the stimulus and wherein the chaperone protein comprises a heat shock protein (“HSP”).
 56. The method of claim 55, wherein the heat shock protein is HSP 70, Hsp30, Hsp60, Hsp90, Hsp94, Hsp96, or Hsp110.
 57. A method for shrinking a distal-nasopharyngeal carcinoma in a subject having the distal-nasopharyngeal carcinoma and a first-nasopharyngeal carcinoma comprising: (a) contacting the a first-nasopharyngeal carcinoma with an isolated oncolytic adenovirus forming a treated carcinoma; (b) waiting a first period of time; (c) applying a stimulus to the treated carcinoma for a second period of time; the stimulus raising a local temperature of the treated carcinoma in a range of about 1 to about 7 degrees Celsius above a normal body temperature of the subject; (d) repeating steps (a), (b), and (c) for a first-number of rounds; and (e) repeating step (c) for a second-number of rounds; wherein, the first period of time is in a range of about 1 to about 10 days; the second period of time is about 15 minutes to about 90 minutes; the first-number of rounds is in a range of 1 to about 5 rounds; the second-number of rounds is in a range of about 1 to about 16 rounds.
 58. The method of claim 57, wherein the isolated oncolytic adenovirus comprises SeqID#1 or SeqID#2.
 59. The method of claim 57, wherein the stimulus is localized to the treated carcinoma and the stimulus is selected from a group consisting of: a high-frequency electromagnetic pulse; a radiofrequency in the range of 0.1 to 100 Mhz; a microwave diathermy in the range of 100 to 2,450 Mhz; or an ultrasound diathermy, wherein the stimulus increases a level of the chaperone protein in the first-tumor and the chaperone protein is Hsp 70, Hsp30, Hsp60, Hsp90, Hsp94, Hsp96, or Hsp110.
 60. An isolated nucleic acid comprising a sequence at least 95% identical to SeqID#1, or a degenerate variant of SEQID#1.
 61. An isolated nucleic acid comprising a sequence at least 95% identical to SeqID#2, or a degenerate variant of SEQID#2. 